Frontonasal malformation with tetralogy of Fallot associated with a submicroscopic deletion of 22q11-Reference-Cited by-同舟云学术

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Frontonasal malformation with tetralogy of Fallot associated with a submicroscopic deletion of 22q11

Published:1997-03-31 Issue:3 Volume:69 Page:287-289
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Stratton Robert F.,Payne René M.

Publisher

Wiley

Subject

Genetics(clinical)

Reference13 articles.

1. , , , , (1988): Frontonasal malformation and dup (2q) syndrome. Am J Med Genet [Suppl 4]: 191–192.

2. Frontonasal dysplasia associated with tetralogy of Fallot.

3. Frontonasal malformation and reciprocal translocation t(15;22)(q22;q13)

4. , (1990): “Syndromes of the Head and Neck”. New York: Oxford Press, pp 785–788.

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1. Nasal Dimple as a Rare Phenotype of Digeroge Syndrome: Revisited;The Indian Journal of Pediatrics;2017-09-19

2. Frontonasal Dysplasia;Atlas of Genetic Diagnosis and Counseling;2017

3. Frontonasal Dysplasia;Atlas of Genetic Diagnosis and Counseling;2016

4. Frontonasal Dysplasia;Atlas of Genetic Diagnosis and Counseling;2012

5. Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization;American Journal of Medical Genetics Part A;2011-09-21

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