Sindrome della quadrupla X (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrome della quadrupla X" in Italian language version.

refsWebsite

Global rank Italian rank

32nih.gov

4^th place

9^th place

31doi.org

2^nd place

7^th place

21oadoi.org

799^th place

22^nd place

5web.archive.org

1^st place

2harvard.edu

18^th place

104^th place

2rarechromo.org

low place

1cdc.gov

218^th place

774^th place

1abs.gov.au

653^rd place

969^th place

1genetic.org

low place

1archive.org

6^th place

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1medlineplus.gov

1,581^st place

5,547^th place

abs.gov.au

Australian Health Survey: First Results, su abs.gov.au, Australian Bureau of Statistics, 29 ottobre 2012. URL consultato il 23 marzo 2021 (archiviato il 20 gennaio 2017).

archive.org

Subrata Kumar Dey e Sujoy Ghosh, Etiology of Down Syndrome: Risk of Advanced Maternal Age and Altered Meiotic Recombination for Chromosome 21 Nondisjunction, in Genetics and Etiology of Down Syndrome, London, IntechOpen, 29 agosto 2011, pp. 23-31, ISBN 978-953-307-631-7.

cdc.gov

US Dept. of Health and Human Services, Anthropometric Reference Data for Children and Adults: United States, 2011–2014 (PDF), in National Health Statistics Reports, vol. 11, agosto 2016. URL consultato il 23 marzo 2021 (archiviato il 2 febbraio 2017).

doi.org

dx.doi.org

Ford CE, Jones KW, Polani PE, ((de Almeida JCC)), Briggs JH, A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome), in Lancet, vol. 273, n. 7075, 1959, pp. 711–713, DOI:10.1016/S0140-6736(59)91893-8, PMID 13642858.
Jacobs PA, Strong JA, A case of human intersexuality having a possible XXY sex-determining mechanism, in Nature, vol. 183, n. 4657, 31 gennaio 1959, pp. 302–303, Bibcode:1959Natur.183..302J, DOI:10.1038/183302a0, PMID 13632697.
Jacobs PA, Baikie AG, Court Brown WM, MacGregor TN, Harnden DG, Evidence for the existence of the human "super female", in Lancet, vol. 274, n. 7100, 26 settembre 1959, pp. 423–425, DOI:10.1016/S0140-6736(59)90415-5, PMID 14406377.
Berg JM, Karlinsky H, Korossy M, Pakula Z, Twenty-six years later: a woman with tetra-X chromosomes, in Journal of Mental Deficiency Research, vol. 32, n. 1, 1988, pp. 67–74, DOI:10.1111/j.1365-2788.1988.tb01389.x, PMID 3361607.
Nielsen J, Homma A, Christiansen F, Rasmussen K, Women with tetra-X (48,XXXX), in Hereditas, vol. 85, n. 2, 1977, pp. 151–156, DOI:10.1111/j.1601-5223.1977.tb00962.x, PMID 885729.
Berkeley MI, Faed MJ, A female with the 48,XXXX karyotype, in Journal of Medical Genetics, vol. 7, n. 1, marzo 1970, pp. 83–85, DOI:10.1136/jmg.7.1.83, PMC 1468910, PMID 5480970.
Ricci N, Dallapiccola B, Ventimiglia B, Tiepolo L, Fraccaro M, 48, XXXX/49, XXXXX mosaic: asynchronies among the late-replicating X chromosomes, in Cytogenetics, vol. 7, n. 4, 1968, pp. 249–259, DOI:10.1159/000129989, PMID 5722744.
Polani PE, Abnormal sex chromosomes and mental disorders, in Nature, vol. 223, n. 5207, 16 agosto 1969, pp. 680–686, Bibcode:1969Natur.223..680P, DOI:10.1038/223680a0, PMID 4896514.
Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L, A review of trisomy X (47,XXX), in Orphanet Journal of Rare Diseases, vol. 5, n. 8, 11 maggio 2010, p. 8, DOI:10.1186/1750-1172-5-8, PMC 2883963, PMID 20459843.
Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P, 48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome, in Acta Paediatrica, vol. 100, n. 6, giugno 2011, pp. 851–860, DOI:10.1111/j.1651-2227.2011.02235.x, PMC 3314712, PMID 21342258.
Samango-Sprouse C, Keen C, Mitchell F, Sadeghin T, Gropman A, Neurodevelopmental Variability in Three Young Girls With a Rare Chromosomal Disorder, 48,XXXX, in American Journal of Medical Genetics Part A, 167A, n. 10, 18 giugno 2015, pp. 2251–2259, DOI:10.1002/ajmg.a.37198, PMID 26086740.
Blackston RD, Chen AT, A case of 48,XXXX female with normal intelligence, in Journal of Medical Genetics, vol. 9, n. 2, giugno 1972, pp. 230–232, DOI:10.1136/jmg.9.2.230, PMC 1469029, PMID 5046634.
Álvarez-Vázquez P, Rivera A, Figueroa I, Páramo C, García-Mayor RV, Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy, in Pituitary, vol. 9, n. 2, 10 luglio 2006, pp. 145–149, DOI:10.1007/s11102-006-9330-0, PMID 16832583.
Schoubben E, Decaestecker K, Quaegebeur K, Danneels L, Mortier G, Cornette L, Tetrasomy and pentasomy of the X chromosome, in European Journal of Pediatrics, vol. 170, n. 10, 18 maggio 2011, pp. 1325–1327, DOI:10.1007/s00431-011-1491-9, PMID 21590264.
Kaur A, Pandi M, Singh JR, 48,XXXX, A Rare Aneuploidy, in Balkan Journal of Medical Genetics, vol. 12, n. 1, 2009, pp. 65–68, DOI:10.2478/v10034-009-0006-8.
Visootsak J, Graham JM, Klinefelter syndrome and other sex chromosomal aneuploidies, in Orphanet Journal of Rare Diseases, vol. 1, n. 1, 24 ottobre 2006, p. 42, DOI:10.1186/1750-1172-1-42, PMC 1634840, PMID 17062147.
Tartaglia N, Howell S, Wilson R, Janusz J, Boada R, Martin S, Frazier JB, Pfeiffer M, Regan K, McSwegin S, Zeitler P, The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy, in Journal of Multidisciplinary Healthcare, vol. 8, n. 1, 17 luglio 2015, pp. 323–334, DOI:10.2147/JMDH.S80242, PMC 4514383, PMID 26229481.
Mandalenakis Z, Giang KW, Eriksson P, Liden H, Synnergren M, Wåhlander H, Fedchenko M, Rosengren A, Dellborg M, Survival in Children With Congenital Heart Disease: Have We Reached a Peak at 97%?, in Journal of the American Heart Association, vol. 9, n. 22, 6 novembre 2020, pp. e017704, DOI:10.1161/JAHA.120.017704, PMC 7763707, PMID 33153356.
Slae M, Heshin-Bekenstein M, Simckes A, Heimer G, Engelhard D, Eisenstein EM, Female polysomy-X and systemic lupus erythematosus, in Seminars in Arthritis and Rheumatism, vol. 43, n. 4, 2014, pp. 508–512, DOI:10.1016/j.semarthrit.2013.07.014, PMID 24012046.
Mikwar M, MacFarlane AJ, Marchetti F, Mechanisms of oocyte aneuploidy associated with advanced maternal age, in Mutation Research/Reviews in Mutation Research, vol. 785, 4 luglio 2020, p. 108320, DOI:10.1016/j.mrrev.2020.108320, PMID 32800274.
Hassold T, Pettay D, May K, Robinson A, Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy, in Human Genetics, vol. 85, n. 6, ottobre 1990, pp. 648–850, DOI:10.1007/bf00193591, PMID 1977687.
Kuliev A, Verlinsky Y, Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis, in Human Reproduction Update, vol. 10, n. 5, 1º ottobre 2004, pp. 401–407, DOI:10.1093/humupd/dmh036, PMID 15319376.
Chiang T, Schultz RM, Lampson MA, Meiotic Origins of Maternal Age-Related Aneuploidy, in Biology of Reproduction, vol. 86, n. 1, 1º gennaio 2012, pp. 1–7, DOI:10.1095/biolreprod.111.094367, PMC 3313661, PMID 21957193.
Bojesen A, Juul S, Gravholt GH, Prenatal and Postnatal Prevalence of Klinefelter Syndrome: A National Registry Study, in Journal of Clinical Endocrinology & Metabolism, vol. 88, n. 2, 1º febbraio 2003, pp. 622–626, DOI:10.1210/jc.2002-021491, PMID 12574191.
Ottesen AM, Aksglaede L, Garn I, Tartaglia N, Tassone F, Gravholt CH, Bojesen A, ((Sørensen K)), ((Jørgensen N)), Rajpert-De Meyts E, Gerdes T, Lind AM, Kjaergaard S, Juul A, Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy, in American Journal of Medical Genetics Part A, 152A, n. 5, maggio 2010, pp. 1206–1212, DOI:10.1002/ajmg.a.33334, PMC 5454803, PMID 20425825.
Rerrick EG, Mosaic XXX/XXXX sex chromosome complement case report and review of literature, in Journal of Mental Deficiency Research, vol. 14, n. 2, 1970, pp. 141–148, DOI:10.1111/j.1365-2788.1970.tb01108.x, PMID 5512214.
Olanders S, Wålinder J, Cutis verticis gyrata in a woman with supernumerary X chromosomes (46,XX/47,XXX/48,XXXX), in Acta Psychiatrica Scandinavica, vol. 46, n. 2, 1970, pp. 120–125, DOI:10.1111/j.1600-0447.1970.tb02107.x, PMID 5478539.
Cirillo Silengo A, Davi GF, Franceschini P, The 49,XXXXX syndrome, in Acta Paediatrica, vol. 68, n. 5, settembre 1979, pp. 769–771, DOI:10.1111/j.1651-2227.1979.tb18456.x.
Nakano S, Sasame A, Azukizawa S, Kigoshi T, Uchida K, Takahashi H, Morimoto S, Pentasomy X mosaic in two adult sisters with diabetes mellitus, in Internal Medicine, vol. 31, n. 9, settembre 1992, pp. 1102–1106, DOI:10.2169/internalmedicine.31.1102, PMID 1421717.
Plaiasu V, Ochiana D, Motei G, Anca IA, A new case of tetrasomy X in a 8 year old girl, in Acta Endocrinologica, vol. 8, n. 4, ottobre 2012, pp. 627–632, DOI:10.4183/aeb.2012.627.
Singer J, Sachdeva S, Smith GF, Hsia JY, Triple X female and a Down's syndrome offspring, in Journal of Medical Genetics, vol. 9, n. 2, giugno 1972, pp. 238–239, DOI:10.1136/jmg.9.2.238, PMC 1469037, PMID 4261628.

genetic.org

AXYS, Berry Kravis E, Seizures and Tremor in People with X & Y Chromosome Variations (PDF), in AXYS: Association for X and Y Chromosome Variations, dicembre 2020. URL consultato il 26 marzo 2021.

harvard.edu

adsabs.harvard.edu

Jacobs PA, Strong JA, A case of human intersexuality having a possible XXY sex-determining mechanism, in Nature, vol. 183, n. 4657, 31 gennaio 1959, pp. 302–303, Bibcode:1959Natur.183..302J, DOI:10.1038/183302a0, PMID 13632697.
Polani PE, Abnormal sex chromosomes and mental disorders, in Nature, vol. 223, n. 5207, 16 agosto 1969, pp. 680–686, Bibcode:1969Natur.223..680P, DOI:10.1038/223680a0, PMID 4896514.

medlineplus.gov

Edens Hurst AC, Zieve D, Conaway B, Karyotyping, in MedlinePlus, 2 aprile 2021. URL consultato il 9 aprile 2021.

nih.gov

ncbi.nlm.nih.gov

Carr DH, Barr ML, Plunkett ER, An XXXX Sex Chromosome Complex in Two Mentally Defective Females, in Canadian Medical Association Journal, vol. 84, n. 3, 21 gennaio 1961, pp. 131–137, PMC 1939166, PMID 13690988.
Ford CE, Jones KW, Polani PE, ((de Almeida JCC)), Briggs JH, A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome), in Lancet, vol. 273, n. 7075, 1959, pp. 711–713, DOI:10.1016/S0140-6736(59)91893-8, PMID 13642858.
Jacobs PA, Strong JA, A case of human intersexuality having a possible XXY sex-determining mechanism, in Nature, vol. 183, n. 4657, 31 gennaio 1959, pp. 302–303, Bibcode:1959Natur.183..302J, DOI:10.1038/183302a0, PMID 13632697.
Jacobs PA, Baikie AG, Court Brown WM, MacGregor TN, Harnden DG, Evidence for the existence of the human "super female", in Lancet, vol. 274, n. 7100, 26 settembre 1959, pp. 423–425, DOI:10.1016/S0140-6736(59)90415-5, PMID 14406377.
Berg JM, Karlinsky H, Korossy M, Pakula Z, Twenty-six years later: a woman with tetra-X chromosomes, in Journal of Mental Deficiency Research, vol. 32, n. 1, 1988, pp. 67–74, DOI:10.1111/j.1365-2788.1988.tb01389.x, PMID 3361607.
Nielsen J, Homma A, Christiansen F, Rasmussen K, Women with tetra-X (48,XXXX), in Hereditas, vol. 85, n. 2, 1977, pp. 151–156, DOI:10.1111/j.1601-5223.1977.tb00962.x, PMID 885729.
Berkeley MI, Faed MJ, A female with the 48,XXXX karyotype, in Journal of Medical Genetics, vol. 7, n. 1, marzo 1970, pp. 83–85, DOI:10.1136/jmg.7.1.83, PMC 1468910, PMID 5480970.
Ricci N, Dallapiccola B, Ventimiglia B, Tiepolo L, Fraccaro M, 48, XXXX/49, XXXXX mosaic: asynchronies among the late-replicating X chromosomes, in Cytogenetics, vol. 7, n. 4, 1968, pp. 249–259, DOI:10.1159/000129989, PMID 5722744.
Linden MG, Bender BG, Robinson A, Sex chromosome tetrasomy and pentasomy, in Pediatrics, vol. 96, n. 4, ottobre 1995, pp. 672–682, PMID 7567329.
Polani PE, Abnormal sex chromosomes and mental disorders, in Nature, vol. 223, n. 5207, 16 agosto 1969, pp. 680–686, Bibcode:1969Natur.223..680P, DOI:10.1038/223680a0, PMID 4896514.
Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L, A review of trisomy X (47,XXX), in Orphanet Journal of Rare Diseases, vol. 5, n. 8, 11 maggio 2010, p. 8, DOI:10.1186/1750-1172-5-8, PMC 2883963, PMID 20459843.
Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P, 48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome, in Acta Paediatrica, vol. 100, n. 6, giugno 2011, pp. 851–860, DOI:10.1111/j.1651-2227.2011.02235.x, PMC 3314712, PMID 21342258.
Samango-Sprouse C, Keen C, Mitchell F, Sadeghin T, Gropman A, Neurodevelopmental Variability in Three Young Girls With a Rare Chromosomal Disorder, 48,XXXX, in American Journal of Medical Genetics Part A, 167A, n. 10, 18 giugno 2015, pp. 2251–2259, DOI:10.1002/ajmg.a.37198, PMID 26086740.
Blackston RD, Chen AT, A case of 48,XXXX female with normal intelligence, in Journal of Medical Genetics, vol. 9, n. 2, giugno 1972, pp. 230–232, DOI:10.1136/jmg.9.2.230, PMC 1469029, PMID 5046634.
Álvarez-Vázquez P, Rivera A, Figueroa I, Páramo C, García-Mayor RV, Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy, in Pituitary, vol. 9, n. 2, 10 luglio 2006, pp. 145–149, DOI:10.1007/s11102-006-9330-0, PMID 16832583.
Schoubben E, Decaestecker K, Quaegebeur K, Danneels L, Mortier G, Cornette L, Tetrasomy and pentasomy of the X chromosome, in European Journal of Pediatrics, vol. 170, n. 10, 18 maggio 2011, pp. 1325–1327, DOI:10.1007/s00431-011-1491-9, PMID 21590264.
Visootsak J, Graham JM, Klinefelter syndrome and other sex chromosomal aneuploidies, in Orphanet Journal of Rare Diseases, vol. 1, n. 1, 24 ottobre 2006, p. 42, DOI:10.1186/1750-1172-1-42, PMC 1634840, PMID 17062147.
Tartaglia N, Howell S, Wilson R, Janusz J, Boada R, Martin S, Frazier JB, Pfeiffer M, Regan K, McSwegin S, Zeitler P, The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy, in Journal of Multidisciplinary Healthcare, vol. 8, n. 1, 17 luglio 2015, pp. 323–334, DOI:10.2147/JMDH.S80242, PMC 4514383, PMID 26229481.
Mandalenakis Z, Giang KW, Eriksson P, Liden H, Synnergren M, Wåhlander H, Fedchenko M, Rosengren A, Dellborg M, Survival in Children With Congenital Heart Disease: Have We Reached a Peak at 97%?, in Journal of the American Heart Association, vol. 9, n. 22, 6 novembre 2020, pp. e017704, DOI:10.1161/JAHA.120.017704, PMC 7763707, PMID 33153356.
Wood A, Kleis L, Toriello H, Cemeroglu AP, Mosaic Pentasomy X/Tetrasomy X Syndrome and Premature Ovarian Failure, in Indian Pediatrics, vol. 48, n. 5, 17 maggio 2011, pp. 402–404, PMID 21654007.
Slae M, Heshin-Bekenstein M, Simckes A, Heimer G, Engelhard D, Eisenstein EM, Female polysomy-X and systemic lupus erythematosus, in Seminars in Arthritis and Rheumatism, vol. 43, n. 4, 2014, pp. 508–512, DOI:10.1016/j.semarthrit.2013.07.014, PMID 24012046.
Mikwar M, MacFarlane AJ, Marchetti F, Mechanisms of oocyte aneuploidy associated with advanced maternal age, in Mutation Research/Reviews in Mutation Research, vol. 785, 4 luglio 2020, p. 108320, DOI:10.1016/j.mrrev.2020.108320, PMID 32800274.
Hassold T, Pettay D, May K, Robinson A, Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy, in Human Genetics, vol. 85, n. 6, ottobre 1990, pp. 648–850, DOI:10.1007/bf00193591, PMID 1977687.
Kuliev A, Verlinsky Y, Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis, in Human Reproduction Update, vol. 10, n. 5, 1º ottobre 2004, pp. 401–407, DOI:10.1093/humupd/dmh036, PMID 15319376.
Chiang T, Schultz RM, Lampson MA, Meiotic Origins of Maternal Age-Related Aneuploidy, in Biology of Reproduction, vol. 86, n. 1, 1º gennaio 2012, pp. 1–7, DOI:10.1095/biolreprod.111.094367, PMC 3313661, PMID 21957193.
Bojesen A, Juul S, Gravholt GH, Prenatal and Postnatal Prevalence of Klinefelter Syndrome: A National Registry Study, in Journal of Clinical Endocrinology & Metabolism, vol. 88, n. 2, 1º febbraio 2003, pp. 622–626, DOI:10.1210/jc.2002-021491, PMID 12574191.
Telfer MA, Richardson CE, Helmken J, Smith GF, Divergent phenotypes among 48,XXXX and 47,XXX females, in American Journal of Human Genetics, vol. 22, n. 3, maggio 1970, pp. 326–335, PMC 1706538, PMID 4392739.
Ottesen AM, Aksglaede L, Garn I, Tartaglia N, Tassone F, Gravholt CH, Bojesen A, ((Sørensen K)), ((Jørgensen N)), Rajpert-De Meyts E, Gerdes T, Lind AM, Kjaergaard S, Juul A, Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy, in American Journal of Medical Genetics Part A, 152A, n. 5, maggio 2010, pp. 1206–1212, DOI:10.1002/ajmg.a.33334, PMC 5454803, PMID 20425825.
Rerrick EG, Mosaic XXX/XXXX sex chromosome complement case report and review of literature, in Journal of Mental Deficiency Research, vol. 14, n. 2, 1970, pp. 141–148, DOI:10.1111/j.1365-2788.1970.tb01108.x, PMID 5512214.
Olanders S, Wålinder J, Cutis verticis gyrata in a woman with supernumerary X chromosomes (46,XX/47,XXX/48,XXXX), in Acta Psychiatrica Scandinavica, vol. 46, n. 2, 1970, pp. 120–125, DOI:10.1111/j.1600-0447.1970.tb02107.x, PMID 5478539.
Nakano S, Sasame A, Azukizawa S, Kigoshi T, Uchida K, Takahashi H, Morimoto S, Pentasomy X mosaic in two adult sisters with diabetes mellitus, in Internal Medicine, vol. 31, n. 9, settembre 1992, pp. 1102–1106, DOI:10.2169/internalmedicine.31.1102, PMID 1421717.
Singer J, Sachdeva S, Smith GF, Hsia JY, Triple X female and a Down's syndrome offspring, in Journal of Medical Genetics, vol. 9, n. 2, giugno 1972, pp. 238–239, DOI:10.1136/jmg.9.2.238, PMC 1469037, PMID 4261628.

oadoi.org

Ford CE, Jones KW, Polani PE, ((de Almeida JCC)), Briggs JH, A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome), in Lancet, vol. 273, n. 7075, 1959, pp. 711–713, DOI:10.1016/S0140-6736(59)91893-8, PMID 13642858.
Jacobs PA, Strong JA, A case of human intersexuality having a possible XXY sex-determining mechanism, in Nature, vol. 183, n. 4657, 31 gennaio 1959, pp. 302–303, Bibcode:1959Natur.183..302J, DOI:10.1038/183302a0, PMID 13632697.
Jacobs PA, Baikie AG, Court Brown WM, MacGregor TN, Harnden DG, Evidence for the existence of the human "super female", in Lancet, vol. 274, n. 7100, 26 settembre 1959, pp. 423–425, DOI:10.1016/S0140-6736(59)90415-5, PMID 14406377.
Berg JM, Karlinsky H, Korossy M, Pakula Z, Twenty-six years later: a woman with tetra-X chromosomes, in Journal of Mental Deficiency Research, vol. 32, n. 1, 1988, pp. 67–74, DOI:10.1111/j.1365-2788.1988.tb01389.x, PMID 3361607.
Nielsen J, Homma A, Christiansen F, Rasmussen K, Women with tetra-X (48,XXXX), in Hereditas, vol. 85, n. 2, 1977, pp. 151–156, DOI:10.1111/j.1601-5223.1977.tb00962.x, PMID 885729.
Ricci N, Dallapiccola B, Ventimiglia B, Tiepolo L, Fraccaro M, 48, XXXX/49, XXXXX mosaic: asynchronies among the late-replicating X chromosomes, in Cytogenetics, vol. 7, n. 4, 1968, pp. 249–259, DOI:10.1159/000129989, PMID 5722744.
Polani PE, Abnormal sex chromosomes and mental disorders, in Nature, vol. 223, n. 5207, 16 agosto 1969, pp. 680–686, Bibcode:1969Natur.223..680P, DOI:10.1038/223680a0, PMID 4896514.
Samango-Sprouse C, Keen C, Mitchell F, Sadeghin T, Gropman A, Neurodevelopmental Variability in Three Young Girls With a Rare Chromosomal Disorder, 48,XXXX, in American Journal of Medical Genetics Part A, 167A, n. 10, 18 giugno 2015, pp. 2251–2259, DOI:10.1002/ajmg.a.37198, PMID 26086740.
Álvarez-Vázquez P, Rivera A, Figueroa I, Páramo C, García-Mayor RV, Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy, in Pituitary, vol. 9, n. 2, 10 luglio 2006, pp. 145–149, DOI:10.1007/s11102-006-9330-0, PMID 16832583.
Schoubben E, Decaestecker K, Quaegebeur K, Danneels L, Mortier G, Cornette L, Tetrasomy and pentasomy of the X chromosome, in European Journal of Pediatrics, vol. 170, n. 10, 18 maggio 2011, pp. 1325–1327, DOI:10.1007/s00431-011-1491-9, PMID 21590264.
Kaur A, Pandi M, Singh JR, 48,XXXX, A Rare Aneuploidy, in Balkan Journal of Medical Genetics, vol. 12, n. 1, 2009, pp. 65–68, DOI:10.2478/v10034-009-0006-8.
Slae M, Heshin-Bekenstein M, Simckes A, Heimer G, Engelhard D, Eisenstein EM, Female polysomy-X and systemic lupus erythematosus, in Seminars in Arthritis and Rheumatism, vol. 43, n. 4, 2014, pp. 508–512, DOI:10.1016/j.semarthrit.2013.07.014, PMID 24012046.
Mikwar M, MacFarlane AJ, Marchetti F, Mechanisms of oocyte aneuploidy associated with advanced maternal age, in Mutation Research/Reviews in Mutation Research, vol. 785, 4 luglio 2020, p. 108320, DOI:10.1016/j.mrrev.2020.108320, PMID 32800274.
Hassold T, Pettay D, May K, Robinson A, Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy, in Human Genetics, vol. 85, n. 6, ottobre 1990, pp. 648–850, DOI:10.1007/bf00193591, PMID 1977687.
Kuliev A, Verlinsky Y, Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis, in Human Reproduction Update, vol. 10, n. 5, 1º ottobre 2004, pp. 401–407, DOI:10.1093/humupd/dmh036, PMID 15319376.
Bojesen A, Juul S, Gravholt GH, Prenatal and Postnatal Prevalence of Klinefelter Syndrome: A National Registry Study, in Journal of Clinical Endocrinology & Metabolism, vol. 88, n. 2, 1º febbraio 2003, pp. 622–626, DOI:10.1210/jc.2002-021491, PMID 12574191.
Rerrick EG, Mosaic XXX/XXXX sex chromosome complement case report and review of literature, in Journal of Mental Deficiency Research, vol. 14, n. 2, 1970, pp. 141–148, DOI:10.1111/j.1365-2788.1970.tb01108.x, PMID 5512214.
Olanders S, Wålinder J, Cutis verticis gyrata in a woman with supernumerary X chromosomes (46,XX/47,XXX/48,XXXX), in Acta Psychiatrica Scandinavica, vol. 46, n. 2, 1970, pp. 120–125, DOI:10.1111/j.1600-0447.1970.tb02107.x, PMID 5478539.
Cirillo Silengo A, Davi GF, Franceschini P, The 49,XXXXX syndrome, in Acta Paediatrica, vol. 68, n. 5, settembre 1979, pp. 769–771, DOI:10.1111/j.1651-2227.1979.tb18456.x.
Nakano S, Sasame A, Azukizawa S, Kigoshi T, Uchida K, Takahashi H, Morimoto S, Pentasomy X mosaic in two adult sisters with diabetes mellitus, in Internal Medicine, vol. 31, n. 9, settembre 1992, pp. 1102–1106, DOI:10.2169/internalmedicine.31.1102, PMID 1421717.
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