Six cases of 7p deletion: Clinical, cytogenetic, and molecular studies-Reference-Cited by-同舟云学术

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Six cases of 7p deletion: Clinical, cytogenetic, and molecular studies

Published:1994-07-01 Issue:3 Volume:51 Page:270-276
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chotai Kokila A.,Brueton Louise A.,van Herwerden Lyn,Garrett Christine,Hinkel Georg K.,Schinzel Albert,Mueller Robert F.,Speleman Frank,Winter Robin M.

Publisher

Wiley

Subject

Genetics(clinical)

Reference37 articles.

1. Chromosome 7p - syndrome: Craniosynostosis with preservation of region 7p2

2. Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7*

3. Interstitial deletion of the short arm of chromosome 7 without craniosynostosis

4. Chromosomal localisation of a developmental gene in man: Direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13

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1. Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review;Genes;2021-10-23

2. Types of Craniosynostosis and their Etiology, Pathophysiology and Epidemiology;The Sutures of the Skull;2021

3. Genetic advances in craniosynostosis;American Journal of Medical Genetics Part A;2017-02-04

4. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017

5. Craniosynostosis: A multidisciplinary approach based on medical, social and demographic factors in a developing country;Revista Médica del Hospital General de México;2016-10

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