Sex linkage (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sex linkage" in English language version.

refsWebsite

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94nih.gov

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acog.org

"Carrier Screening". www.acog.org. Retrieved 10 March 2025.

alportsyndromenews.com

Zaunbrecher, Nicole. "Types of Alport Syndrome - Alport Syndrome News". alportsyndromenews.com. Retrieved 28 March 2025.

annualreviews.org

Hughes, Jennifer F.; Page, David C. (23 November 2015). "The Biology and Evolution of Mammalian Y Chromosomes". Annual Review of Genetics. 49: 507–527. doi:10.1146/annurev-genet-112414-055311. hdl:1721.1/108037. ISSN 0066-4197. PMID 26442847.
Hughes, Jennifer F.; Page, David C. (23 November 2015). "The Biology and Evolution of Mammalian Y Chromosomes". Annual Review of Genetics. 49 (2015): 507–527. doi:10.1146/annurev-genet-112414-055311. hdl:1721.1/108037. ISSN 0066-4197. PMID 26442847.

asu.edu

embryo.asu.edu

"Studies in Spermatogenesis (1905), by Nettie Maria Stevens | Embryo Project Encyclopedia". embryo.asu.edu. Retrieved 4 April 2025.
""Sex Limited Inheritance in Drosophila" (1910), by Thomas Hunt Morgan | Embryo Project Encyclopedia". embryo.asu.edu. Retrieved 4 April 2025.

bleeding.org

"Hemophilia A Overview: Symptoms, Genetics, Treatments". National Bleeding Disorders Foundation. Retrieved 25 March 2025.

cancer.gov

"NCI Dictionary of Genetics Terms". National Cancer Institute. 21 March 2025.

cell.com

Bachtrog, Doris; Kirkpatrick, Mark; Mank, Judith E.; McDaniel, Stuart F.; Pires, J. Chris; Rice, William; Valenzuela, Nicole (1 September 2011). "Are all sex chromosomes created equal?". Trends in Genetics. 27 (9): 350–357. doi:10.1016/j.tig.2011.05.005. ISSN 0168-9525. PMID 21962970.

clevelandclinic.org

my.clevelandclinic.org

"Duchenne Muscular Dystrophy (DMD)". Cleveland Clinic. 25 July 2022. Retrieved 22 March 2025.
"What Is Fragile X Syndrome (FXS)?". Cleveland Clinic. Archived from the original on 13 February 2025. Retrieved 10 March 2025.

core.ac.uk

Dever, Jennifer (2024). "Female Biology". All USF Faculty Authored Books: 54–107.

doi.org

Kumar, Rahul; Gautam, Akash; Singh, Shashi Bala (2020), "Sex-Linked", in Vonk, Jennifer; Shackelford, Todd (eds.), Encyclopedia of Animal Cognition and Behavior, Cham: Springer International Publishing, pp. 1–4, doi:10.1007/978-3-319-47829-6_562-1, ISBN 978-3-319-47829-6, retrieved 10 March 2025
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Shvetsova, Ekaterina; Sofronova, Alina; Monajemi, Ramin; Gagalova, Kristina; Draisma, Harmen H. M.; White, Stefan J.; Santen, Gijs W. E.; Chuva de Sousa Lopes, Susana M.; Heijmans, Bastiaan T.; van Meurs, Joyce; Jansen, Rick; Franke, Lude; Kiełbasa, Szymon M.; den Dunnen, Johan T.; ‘t Hoen, Peter A. C. (14 December 2018). "Skewed X-inactivation is common in the general female population". European Journal of Human Genetics. 27 (3): 455–465. doi:10.1038/s41431-018-0291-3. PMC 6460563. PMID 30552425.
Jais, Jean Philippe; Knebelmann, Bertrand; Giatras, Iannis; De Marchi, Mario; Rizzoni, Gianfranco; Renieri, Alessandra; Weber, Manfred; Gross, Oliver; Netzer, Kai-Olaf; Flinter, Frances; Pirson, Yves; Dahan, Karin; Wieslander, Jörgen; Persson, Ulf; Tryggvason, Karl; Martin, Paula; Hertz, Jens Michael; Schröder, Cornelis; Sanak, Marek; Carvalho, Maria Fernanda; Saus, Juan; Antignac, Corinne; Smeets, Hubert; Gubler, Marie Claire (October 2003). "X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A 'European Community Alport Syndrome Concerted Action' Study". Journal of the American Society of Nephrology. 14 (10): 2603–2610. doi:10.1097/01.ASN.0000090034.71205.74. PMID 14514738.
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Seager, M. J.; Whatley, S. D.; Anstey, A. V.; Millard, T. P. (2014). "X-linked dominant protoporphyria: a new porphyria". Clinical and Experimental Dermatology. 39 (1): 35–37. doi:10.1111/ced.12202. PMID 24131146.
Nozu, Kandai; Nakanishi, Koichi; Abe, Yoshifusa; Udagawa, Tomohiro; Okada, Shinichi; Okamoto, Takayuki; Kaito, Hiroshi; Kanemoto, Katsuyoshi; Kobayashi, Anna; Tanaka, Eriko; Tanaka, Kazuki; Hama, Taketsugu; Fujimaru, Rika; Miwa, Saori; Yamamura, Tomohiko (February 2019). "A review of clinical characteristics and genetic backgrounds in Alport syndrome". Clinical and Experimental Nephrology. 23 (2): 158–168. doi:10.1007/s10157-018-1629-4. ISSN 1437-7799. PMC 6510800. PMID 30128941.
McLennan, Yingratana; Polussa, Jonathan; Tassone, Flora; Hagerman, Randi (May 2011). "Fragile x syndrome". Current Genomics. 12 (3): 216–224. doi:10.2174/138920211795677886. ISSN 1875-5488. PMC 3137006. PMID 22043169.
Bartholomay, Kristi L.; Lee, Cindy H.; Bruno, Jennifer L.; Lightbody, Amy A.; Reiss, Allan L. (12 January 2019). "Closing the Gender Gap in Fragile X Syndrome: Review on Females with FXS and Preliminary Research Findings". Brain Sciences. 9 (1): 11. doi:10.3390/brainsci9010011. ISSN 2076-3425. PMC 6356553. PMID 30642066.
Garber, Kathryn B.; Visootsak, Jeannie; Warren, Stephen T. (June 2008). "Fragile X syndrome". European Journal of Human Genetics. 16 (6): 666–672. doi:10.1038/ejhg.2008.61. ISSN 1018-4813. PMC 4369150. PMID 18398441.
Hogan, Andrew J. (1 June 2012). "Visualizing carrier status: Fragile X syndrome and genetic diagnosis since the 1940s". Endeavour. 36 (2): 77–84. doi:10.1016/j.endeavour.2011.12.002. PMID 22257912.
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Schwartzman, J. S.; Bernardino, Andrea; Nishimura, Agnes; Gomes, Raquel R.; Zatz, Mayana (June 2001). "Rett Syndrome in a Boy with a 47,XXY Karyotype Confirmed by a Rare Mutation in the MECP2 Gene". Neuropediatrics. 32 (3): 162–164. doi:10.1055/s-2001-16620. ISSN 0174-304X. PMID 11521215.
Saito, Tasuku; Nishii, Yutaka; Yasuda, Toshiyuki; Ito, Nobuaki; Suzuki, Hisanori; Igarashi, Takashi; Fukumoto, Seiji; Fujita, Toshiro (1 October 2009). "Familial hypophosphatemic rickets caused by a large deletion in PHEX gene". European Journal of Endocrinology. 161 (4): 647–651. doi:10.1530/EJE-09-0261. ISSN 0804-4643. PMID 19581284.
Barros, Nilana MT; Hoac, Betty; Neves, Raquel L; Addison, William N; Assis, Diego M; Murshed, Monzur; Carmona, Adriana K; McKee, Marc D (1 March 2013). "Proteolytic processing of osteopontin by PHEX and accumulation of osteopontin fragments in Hyp mouse bone, the murine model of X-linked hypophosphatemia". Journal of Bone and Mineral Research. 28 (3): 688–699. doi:10.1002/jbmr.1766. ISSN 0884-0431. PMID 22991293.
Boukpessi, Tchilalo; Hoac, Betty; Coyac, Benjamin R.; Leger, Thibaut; Garcia, Camille; Wicart, Philippe; Whyte, Michael P.; Glorieux, Francis H.; Linglart, Agnès; Chaussain, Catherine; McKee, Marc D. (1 February 2017). "Osteopontin and the dento-osseous pathobiology of X-linked hypophosphatemia". Bone. 95: 151–161. doi:10.1016/j.bone.2016.11.019. ISSN 8756-3282.
McKee, Marc D.; Buss, Daniel J.; Reznikov, Natalie (1 March 2022). "Mineral tessellation in bone and the stenciling principle for extracellular matrix mineralization". Journal of Structural Biology. 214 (1): 107823. doi:10.1016/j.jsb.2021.107823. ISSN 1047-8477. PMID 34915130.
Carpenter, Thomas O. (1 April 1997). "New Perspectives on the Biology and Treatment of X-Linked Hypophosphatemic Rickets". Pediatric Clinics of North America. 44 (2): 443–466. doi:10.1016/S0031-3955(05)70485-5. ISSN 0031-3955.
Linglart, Agnès; Biosse-Duplan, Martin; Briot, Karine; Chaussain, Catherine; Esterle, Laure; Guillaume-Czitrom, Séverine; Kamenicky, Peter; Nevoux, Jerome; Prié, Dominique; Rothenbuhler, Anya; Wicart, Philippe; Harvengt, Pol (2014). "Therapeutic management of hypophosphatemic rickets from infancy to adulthood". Endocrine Connections. 3 (1): R13–30. doi:10.1530/EC-13-0103. ISSN 2049-3614. PMC 3959730. PMID 24550322.
Haffner, Dieter; Emma, Francesco; Eastwood, Deborah M.; Biosse Duplan, Martin; Bacchetta, Justine; Schnabel, Dirk; Wicart, Philippe; Bockenhauer, Detlef; Santos, Fernando; Levtchenko, Elena; Harvengt, Pol; Kirchhoff, Martha; Di Rocco, Federico; Chaussain, Catherine; Brandi, Maria Louisa (July 2019). "Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia". Nature Reviews. Nephrology. 15 (7): 435–455. doi:10.1038/s41581-019-0152-5. ISSN 1759-507X. PMC 7136170. PMID 31068690.
Imel, Erik A.; DiMeglio, Linda A.; Hui, Siu L.; Carpenter, Thomas O.; Econs, Michael J. (April 2010). "Treatment of X-linked hypophosphatemia with calcitriol and phosphate increases circulating fibroblast growth factor 23 concentrations". The Journal of Clinical Endocrinology and Metabolism. 95 (4): 1846–1850. doi:10.1210/jc.2009-1671. ISSN 1945-7197. PMC 2853995. PMID 20157195.
Ewert, Annika; Rehberg, Mirko; Schlingmann, Karl Peter; Hiort, Olaf; John-Kroegel, Ulrike; Metzing, Oliver; Wühl, Elke; Schaefer, Franz; Kemper, Markus J; Derichs, Ute; Richter-Unruh, Annette; Patzer, Ludwig; Albers, Norbert; Dunstheimer, Desiree; Haberland, Holger (1 October 2023). "Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia". The Journal of Clinical Endocrinology & Metabolism. 108 (10): e998 – e1006. doi:10.1210/clinem/dgad223. ISSN 0021-972X. PMID 37097907.
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"Pavone P, Praticò AD, Falsaperla R, Ruggieri M, Zollino M, Corsello G, Neri G. Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes. Ital J Pediatr. 2015 Aug 5;41:55. doi: 10.1186/s13052-015-0161-3. PMID: 26242548; PMCID: PMC4526284". doi:10.1186/s13052-015-0161-3. {{cite web}}: Missing or empty |url= (help)
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elsevier.com

linkinghub.elsevier.com

Skuse, David; Printzlau, Frida; Wolstencroft, Jeanne (1 January 2018), Geschwind, Daniel H.; Paulson, Henry L.; Klein, Christine (eds.), "Chapter 24 - Sex chromosome aneuploidies", Handbook of Clinical Neurology, Neurogenetics, Part I, vol. 147, Elsevier, pp. 355–376, doi:10.1016/b978-0-444-63233-3.00024-5, ISBN 978-0-444-63233-3, PMID 29325624, retrieved 27 March 2025

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genome.gov

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gimjournal.org

Gregg, Anthony R.; Aarabi, Mahmoud; Klugman, Susan; Leach, Natalia T.; Bashford, Michael T.; Goldwaser, Tamar; Chen, Emily; Sparks, Teresa N.; Reddi, Honey V.; Rajkovic, Aleksandar; Dungan, Jeffrey S. (1 October 2021). "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)". Genetics in Medicine. 23 (10): 1793–1806. doi:10.1038/s41436-021-01203-z. ISSN 1098-3600. PMC 8488021. PMID 34285390.

handle.net

hdl.handle.net

Hughes, Jennifer F.; Page, David C. (23 November 2015). "The Biology and Evolution of Mammalian Y Chromosomes". Annual Review of Genetics. 49: 507–527. doi:10.1146/annurev-genet-112414-055311. hdl:1721.1/108037. ISSN 0066-4197. PMID 26442847.
Hughes, Jennifer F.; Page, David C. (23 November 2015). "The Biology and Evolution of Mammalian Y Chromosomes". Annual Review of Genetics. 49 (2015): 507–527. doi:10.1146/annurev-genet-112414-055311. hdl:1721.1/108037. ISSN 0066-4197. PMID 26442847.

harvard.edu

ui.adsabs.harvard.edu

Hunt, David M.; Dulai, Kanwaijit S.; Bowmaker, James K.; Mollon, John D. (17 February 1995). "The Chemistry of John Dalton's Color Blindness". Science. 267 (5200): 984–988. Bibcode:1995Sci...267..984H. doi:10.1126/science.7863342. ISSN 0036-8075. PMID 7863342.
Mallet J.; Joron M. (1999). "The evolution of diversity in warning color and mimicry: polymorphisms, shifting balance, and speciation". Annual Review of Ecology and Systematics. 30 (1): 201–233. Bibcode:1999AnRES..30..201M. doi:10.1146/annurev.ecolsys.30.1.201.

jcdr.net

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karger.com

Okashita, Naoki; Tachibana, Makoto (28 September 2021). "Transcriptional Regulation of the Y-Linked Mammalian Testis-Determining Gene SRY". Sexual Development. 15 (5–6): 351–359. doi:10.1159/000519217. ISSN 1661-5425. PMID 34583357.

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mayoclinic.org

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