Σύνδρομο Κλαϊνφέλτερ (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Σύνδρομο Κλαϊνφέλτερ" in Greek language version.

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8nih.gov

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4doi.org

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3archive.org

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archive.org

Klinefelter, HF Jr; Reifenstein, EC Jr; Albright, F. (1942). «Syndrome characterized by gynecomastia, aspermatogenesis without a-Leydigism and increased excretion of follicle-stimulating hormone». J Clin Endocrinol Metab 2 (11): 615–624. doi:10.1210/jcem-2-11-615. https://archive.org/details/sim_journal-of-clinical-endocrinology-and-metabolism_1942-11_2_11/page/615 . Klinefelter, HF (1986). «Klinefelter syndrome: historical background and development». South Med J 79 (45): 1089–1093. doi:10.1097/00007611-198609000-00012. PMID 3529433 talks about the history of the development of the literature.
Jacobs PA, Strong JA (January 31, 1959). «A case of human intersexuality having a possible XXY sex-determining mechanism». Nature 183 (4657): 302–3. doi:10.1038/183302a0. PMID 13632697. https://archive.org/details/sim_nature-uk_1959-01-31_183_4657/page/n35.
Jacobs PA (September 1982). «The William Allan Memorial Award address: human population cytogenetics: the first twenty-five years». Am J Hum Genet 34 (5): 689–98. PMID 6751075. PMC 1685430. https://archive.org/details/sim_american-journal-of-human-genetics_1982-09_34_5/page/689.

archive.today

The Focus Foundation. X & Y Variations. thefocusfoundation.org Αρχειοθετήθηκε 2013-01-13 at Archive.is

doi.org

dx.doi.org

Klinefelter, HF Jr; Reifenstein, EC Jr; Albright, F. (1942). «Syndrome characterized by gynecomastia, aspermatogenesis without a-Leydigism and increased excretion of follicle-stimulating hormone». J Clin Endocrinol Metab 2 (11): 615–624. doi:10.1210/jcem-2-11-615. https://archive.org/details/sim_journal-of-clinical-endocrinology-and-metabolism_1942-11_2_11/page/615 . Klinefelter, HF (1986). «Klinefelter syndrome: historical background and development». South Med J 79 (45): 1089–1093. doi:10.1097/00007611-198609000-00012. PMID 3529433 talks about the history of the development of the literature.
Chow J, Yen Z, Ziesche S, Brown C (2005). «Silencing of the mammalian X chromosome». Annu Rev Genomics Hum Genet 6: 69–92. doi:10.1146/annurev.genom.6.080604.162350. PMID 16124854.
Blaschke RJ, Rappold G (2006). «The pseudoautosomal regions, SHOX and disease. Curr Opin Genet Dev». Jun; 16 (3): 233–9. doi:10.1016/j.gde.2006.04.004. PMID 16650979.
Jacobs PA, Strong JA (January 31, 1959). «A case of human intersexuality having a possible XXY sex-determining mechanism». Nature 183 (4657): 302–3. doi:10.1038/183302a0. PMID 13632697. https://archive.org/details/sim_nature-uk_1959-01-31_183_4657/page/n35.

nih.gov

ncbi.nlm.nih.gov

Klinefelter, HF Jr; Reifenstein, EC Jr; Albright, F. (1942). «Syndrome characterized by gynecomastia, aspermatogenesis without a-Leydigism and increased excretion of follicle-stimulating hormone». J Clin Endocrinol Metab 2 (11): 615–624. doi:10.1210/jcem-2-11-615. https://archive.org/details/sim_journal-of-clinical-endocrinology-and-metabolism_1942-11_2_11/page/615 . Klinefelter, HF (1986). «Klinefelter syndrome: historical background and development». South Med J 79 (45): 1089–1093. doi:10.1097/00007611-198609000-00012. PMID 3529433 talks about the history of the development of the literature.
Chow J, Yen Z, Ziesche S, Brown C (2005). «Silencing of the mammalian X chromosome». Annu Rev Genomics Hum Genet 6: 69–92. doi:10.1146/annurev.genom.6.080604.162350. PMID 16124854.
Blaschke RJ, Rappold G (2006). «The pseudoautosomal regions, SHOX and disease. Curr Opin Genet Dev». Jun; 16 (3): 233–9. doi:10.1016/j.gde.2006.04.004. PMID 16650979.
Jacobs PA, Strong JA (January 31, 1959). «A case of human intersexuality having a possible XXY sex-determining mechanism». Nature 183 (4657): 302–3. doi:10.1038/183302a0. PMID 13632697. https://archive.org/details/sim_nature-uk_1959-01-31_183_4657/page/n35.
Jacobs PA (September 1982). «The William Allan Memorial Award address: human population cytogenetics: the first twenty-five years». Am J Hum Genet 34 (5): 689–98. PMID 6751075. PMC 1685430. https://archive.org/details/sim_american-journal-of-human-genetics_1982-09_34_5/page/689.

nichd.nih.gov

«Klinefelter Syndrome». Health Information. National Institute of Health and Human Development. 19 Φεβρουαρίου 2007. Ανακτήθηκε στις 24 Μαρτίου 2007. and «Klinefelter syndrome». Genetics Home Reference. National Library of Medicine. 2006. Αρχειοθετήθηκε από το πρωτότυπο στις 23 Μαρτίου 2007. Ανακτήθηκε στις 24 Μαρτίου 2007. both provide statistical estimates.

ghr.nlm.nih.gov

«Klinefelter Syndrome». Health Information. National Institute of Health and Human Development. 19 Φεβρουαρίου 2007. Ανακτήθηκε στις 24 Μαρτίου 2007. and «Klinefelter syndrome». Genetics Home Reference. National Library of Medicine. 2006. Αρχειοθετήθηκε από το πρωτότυπο στις 23 Μαρτίου 2007. Ανακτήθηκε στις 24 Μαρτίου 2007. both provide statistical estimates.

pubmedcentral.nih.gov

Jacobs PA (September 1982). «The William Allan Memorial Award address: human population cytogenetics: the first twenty-five years». Am J Hum Genet 34 (5): 689–98. PMID 6751075. PMC 1685430. https://archive.org/details/sim_american-journal-of-human-genetics_1982-09_34_5/page/689.

thefocusfoundation.org

The Focus Foundation. X & Y Variations. thefocusfoundation.org Αρχειοθετήθηκε 2013-01-13 at Archive.is

web.archive.org

«Klinefelter Syndrome». Health Information. National Institute of Health and Human Development. 19 Φεβρουαρίου 2007. Ανακτήθηκε στις 24 Μαρτίου 2007. and «Klinefelter syndrome». Genetics Home Reference. National Library of Medicine. 2006. Αρχειοθετήθηκε από το πρωτότυπο στις 23 Μαρτίου 2007. Ανακτήθηκε στις 24 Μαρτίου 2007. both provide statistical estimates.