A Single Base Pair Mutation Encoding a Premature Stop Codon in the MIS Type II Receptor Is Responsible for Canine Persistent Mullerian Duct Syndrome-Reference-Cited by-同舟云学术

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A Single Base Pair Mutation Encoding a Premature Stop Codon in the MIS Type II Receptor Is Responsible for Canine Persistent Mullerian Duct Syndrome

Published:2008-08-21 Issue:1 Volume:30 Page:46-56
ISSN:0196-3635
Container-title:Journal of Andrology
language:en
Short-container-title:Journal of Andrology

Author:

Wu X.,Wan S.,Pujar S.,Haskins M. E.,Schlafer D. H.,Lee M. M.,Meyers-Wallen V. N.

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

Cited by 53 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. Lack of causative mutation in the AMH and AMHR2 genes in a cat (38,XY) with persistent Mullerian duct syndrome (PMDS);Reproduction in Domestic Animals;2024-06

2. Case report: Persistent Müllerian duct syndrome and enlarged prostatic utricle in a male dog;Frontiers in Veterinary Science;2023-07-04

3. Persisting Wolffian and Müllerian ducts in female and male southern tamanduas (Tamandua tetradactyla)?;Theriogenology Wild;2023

4. The Persistent Müllerian Duct Syndrome;Genetic Steroid Disorders;2023

5. Whole genome sequencing identifies a missense polymorphism in PADI6 associated with testicular/ovotesticular XX disorder of sex development in dogs;Genomics;2022-07

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