Del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21-Reference-Cited by-同舟云学术

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Del(X) (q26) in a phenotypically normal woman and her daughter who also has trisomy 21

Published:1983-02 Issue:2 Volume:14 Page:367-372
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Taysi Kutay,Opitz John M.

Publisher

Wiley

Subject

Genetics (clinical)

Reference15 articles.

1. A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea

2. Deletion mapping of the human X chromosome

3. Fertility in 47,XXX and 45,X patients.

4. X LONG-ARM DELETION WITH FEATURES OF TURNER'S SYNDROME

5. Congenital dislocation of the knees in a child with Down-mosaic Turner syndrome

Cited by 16 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. Chromosome Heteromorphism (Summaries);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

2. Euchromatic Variants;Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

3. Outcome of Spontaneous Pregnancy in Turner Syndrome;Acta Endocrinologica (Bucharest);2015

4. Euchromatic Variants;Human Chromosome Variation: Heteromorphism and Polymorphism;2011

5. Chromosome X;Human Chromosome Variation: Heteromorphism and Polymorphism;2011

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