Newborn infant with del(9)(pter→q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary ears-Reference-Cited by-同舟云学术

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Newborn infant with del(9)(pter→q32:) and multiple congenital anomalies including arrhinencephaly, cardiac malformations, and rudimentary ears

Published:1987 Issue:S3 Volume:28 Page:161-166
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kargas Steve A.,Kargas George A.,Chandra Sunita,Wu Shi-Qi,Meisner Lorraine F.,Opitz John M.,Bernstein Jay

Publisher

Wiley

Subject

Genetics (clinical)

Reference10 articles.

1. (1981): “Manual of Pediatric Physical Diagnosis” Chicago: Yearbook Medical Publishers, pp 260-262.

2. Oncogenes

3. (1984): In (ed): “Anthropometric Measurements of the Newborn Infant (27-41 Gestational Weeks)” White Plains, NY:

Cited by 5 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. Discordant Semilobar Holoprosencephaly in Monozygotic Twins with de novo inv dup(15) Marker Chromosome and de novo Mutation on SHH Gene;Fetal Diagnosis and Therapy;2007

2. Deletion 4q21/4q22 syndrome: Two patients with de novo 4q21.3q23 and 4q13.2q23 deletions;American Journal of Medical Genetics;1997-04-14

3. Paracentric inversion involving the long arm of chromosome 9 resulting in deletion of abl gene;American Journal of Medical Genetics;1997-02-11

4. Infant with multiple congenital anomalies and deletion (9)(q34.3);American Journal of Medical Genetics;1994-06-01

5. Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly;American Journal of Medical Genetics;1989-10

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