Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformations-Reference-Cited by-同舟云学术

Novel mosaic SRY gene deletions in three newborn males with variable genitourinary malformations

Published:2018-07-28 Issue:9 Volume:176 Page:2017-2023
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Roberts Jennifer¹,Lyalin Dmitry¹,Tosatto Norwood¹,Rana Pratibha²³,Fadoul Hiba²³,Welsh Holly³⁴,Zhang Lei¹³,Cooley Linda¹³,Repnikova Elena¹³^ORCID

Affiliation:

1. Department of Pathology & Laboratory Medicine, Division of Clinical Laboratory Genetics & GenomicsThe University of Missouri‐Kansas City School of Medicine Kansas City Missouri

2. Department of Pediatric EndocrinologyThe University of Missouri‐Kansas City School of Medicine Kansas City Missouri

3. Children's Mercy HospitalThe University of Missouri‐Kansas City School of Medicine Kansas City Missouri

4. Division of Clinical GeneticsThe University of Missouri‐Kansas City School of Medicine Kansas City Missouri

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.40428

Reference27 articles.

1. Pre- and postnatal findings in a boy with duplication of the bladder and intestine: Report and review

2. Detection of low-level mosaicism by array CGH in routine diagnostic specimens

3. Partial caudal duplication in a newborn associated with meningomyelocele and complex heart anomaly

4. A novel postzygotic nonsense mutation in SRY in familial XY gonadal dysgenesis

5. The Genetic and Environmental Factors Underlying Hypospadias

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