Cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter→q32:)]
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Two different chromosome abnormalities resulting from a translocation carrier father
2. Two unrelated children with distal long arm deletion of chromosome 7: clinical features, cytogenetic and gene marker studies
3. (1977): “Clinical Atlas of Human Chromosomes.” New York: John Wiley.
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1. Prenatal diagnosis of de novo monosomy 7q33-qter associated with hydrops fetalis, semilobar holoprosencephaly, and premaxillary dysgenesis;Taiwanese Journal of Obstetrics and Gynecology;2013-12
2. Airway Management in an Infant with Alobar Holoprosencephaly and Cebocephaly Associated with Maternal Diabetes Mellitus;Ear, Nose & Throat Journal;2013-05
3. Airway Management in an Infant with Alobar Holoprosencephaly and Cebocephaly Associated with Maternal Diabetes Mellitus;Ear, Nose & Throat Journal;2013-04
4. The interstitial deletion of bands q33-35 of long arm of chromosome 7: a review with a new case report;Clinical Genetics;2008-06-28
5. Malformations in a child with dup (7 pter-p15.1) and del (7 q36-qter) as a result of familial pericentric inversion;Clinical Genetics;2008-06-28
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