Unique Karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian Patient with Ovotesticular Disorder of Sexual Development-Reference-Cited by-同舟云学术

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Unique Karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian Patient with Ovotesticular Disorder of Sexual Development

Published:2013 Issue: Volume: Page:
ISSN:1661-5433
Container-title:Sexual Development
language:en
Short-container-title:Sex Dev

Author:

Mazen I.M.,Kamel A.K.,Mohamed A.M.,Hussien H.A.,Essawi M.L.,Hassan H.A.,El-Ruby M.O.,Aref A.,Mekkawy M.K.

Publisher

S. Karger AG

Subject

Developmental Biology,Embryology,Endocrinology, Diabetes and Metabolism

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Comprehensive analysis of three female patients with different types of X/Y translocations and literature review;Molecular Cytogenetics;2023-05-18

2. A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221);Genes;2022-12-27

3. Cellular fate of intersex differentiation;Cell Death & Disease;2021-04

4. Cytogenetic Spectrum of Ovotesticular Difference of Sex Development (OT DSD) among a Large Cohort of DSD Patients and Literature Review;Sexual Development;2019

5. Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis;Molecular Cytogenetics;2016-08-31

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