Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith Syndrome-Reference-Cited by-同舟云学术

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Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith Syndrome

Published:2001 Issue:2 Volume:104 Page:120-126
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Barr C.L.,Best L.,Weksberg R.

Publisher

Wiley

Subject

Genetics(clinical)

Reference34 articles.

1. 1963. Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of the kidneys and pancreas, and leydig cell hyperplasia: another syndrome? Vol. 11. Los Angeles, California: Transaction of Western Society for Pediatric Research.

2. Familial posterior helical ear pits and Wiedemann-Beckwith syndrome

3. Wiedemann-Beckwith syndrome: Autosomal-dominant inheritance in a family

4. Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups

5. An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

Cited by 9 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. Naevi and other Developmental Defects;Rook's Textbook of Dermatology;2010-05-06

2. Isolated familial posterior earlobe indentations;American Journal of Medical Genetics Part A;2009-03-12

3. Principles of Genetics and Their Clinical Application in the Neonatal Intensive Care Unit;Critical Care Nursing Clinics of North America;2009-03

4. Posterior helical pits;European Journal of Medical Genetics;2007-03

5. Familial posterior helical ear pits;American Journal of Medical Genetics Part A;2007

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