Prenatal diagnosis of a dup(3p) with holoprosencephaly-Reference-Cited by-同舟云学术

Prenatal diagnosis of a dup(3p) with holoprosencephaly

Published:1987-01 Issue:1 Volume:26 Page:225-227
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gillerot Yves,Hustin Jean,Koulischer Lucien,Viteux Vincent,Neri Giovanni,Opitz John M.

Publisher

Wiley

Subject

Genetics (clinical)

Reference6 articles.

1. Dup(3)(p2→pter) in two families, including one infant with cyclopia

2. The dup(3)(p25 → pter) syndrome: A case with holoprosencephaly

3. (1982): Developmental and other pathologic changes in syndromes caused by chromosome abnormalities, Ch. 1 In (eds): “Perspectives in Pediatric Pathology”. Vol 7. New York: Masson Publishing USA, Inc. pp 1-;63.

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1. Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features;Case Reports in Genetics;2019-07-25

2. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature;Taiwanese Journal of Obstetrics and Gynecology;2015-06

3. A patient with a duplication of chromosome 3p (p24.1p26.2): A comparison with other partial 3p trisomies;American Journal of Medical Genetics Part A;2013-12-05

4. Prenatal Diagnosis of Partial Trisomy 3p (3p21→pter) and Partial Monosomy 11q (11q23→qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System;Journal of the Formosan Medical Association;2008-10

5. Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephaly;Clinical Genetics;2008-06-28