Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
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1. Wolf–Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly;Taiwanese Journal of Obstetrics and Gynecology;2020-05
2. Syndromes associated with holoprosencephaly;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-05-17
3. 2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay;European Journal of Medical Genetics;2012-03
4. The Wolf-Hirschhorn Syndrome in Fetal Autopsy - A Case Report -;The Korean Journal of Pathology;2011
5. L;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
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