Incidence of Y chromosome microdeletions in patients with Klinefelter syndrome-Reference-Cited by-同舟云学术

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Incidence of Y chromosome microdeletions in patients with Klinefelter syndrome

Published:2018-11-29 Issue:7 Volume:42 Page:833-842
ISSN:1720-8386
Container-title:Journal of Endocrinological Investigation
language:en
Short-container-title:J Endocrinol Invest

Author:

Sciarra F.,Pelloni M.,Faja F.,Pallotti F.,Martino G.,Radicioni A. F.,Lenzi A.,Lombardo F.,Paoli D.

Funder

MIUR

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/s40618-018-0989-7.pdf

Reference76 articles.

1. Lanfranco F, Kamischke A, Zitzmann M, Nieschlag E (2004) Klinefelter’s syndrome. Lancet 364:273–283

2. Bonomi M, Rochira V, Pasquali D, Balercia G, Jannini EA, Ferlin A, Klinefelter ItaliaN Group (KING) (2017) Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism. J Endocrinol Invest 40:123–134

3. Bojesen A, Juul S, Gravholt CH (2003) Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J Clin Endocrinol Metab 88:622–626

4. Aksglaede L, Wikström AM, Rajpert-De Meyts E, Dunkel L, Skakkebaek NE, Juul A (2006) Natural history of seminiferous tubule degeneration in Klinefelter syndrome. Hum Reprod Update 12:39–48

5. Krausz C, Forti G (2006) Sperm cryopreservation in male infertility due to genetic disorders. Cell Tissue Bank. 7:105–112

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1. Seminological, Hormonal and Ultrasonographic Features of Male Factor Infertility Due to Genetic Causes: Results from a Large Monocentric Retrospective Study;Journal of Clinical Medicine;2024-07-27

2. New Insights beyond Established Norms: A Scoping Review of Genetic Testing for Infertile Men;UROL J;2024

3. Investigating Cytogenetic Profiles in Couples Experiencing Recurrent Implantation Failure Post<i> in vitro</i> Fertilization;OBM Genetics;2024-01-17

4. Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia;BMC Medical Genomics;2023-09-08

5. EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: State of the art 2023;Andrology;2023-09-06

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