The 6p deletion syndrome: a new orofacial clefting syndrome and its implications for antenatal screening
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,Surgery
Reference24 articles.
1. Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6;Eiberg;Clin Genet,1987
2. 1q32-q41 microdeletion with reference to Van der Woude syndrome and allied clefting entities;Houdayer;Am J Med Genet,2000
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2. Rare earth elements in umbilical cord and risk for orofacial clefts;Ecotoxicology and Environmental Safety;2021-01
3. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family;BMC Medical Genomics;2015-07-15
4. Association of JARID2 polymorphisms with non-syndromic orofacial clefts in northern Chinese Han population;Journal of Oral Pathology & Medicine;2014-08-26
5. 6p25 Interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder;European Journal of Paediatric Neurology;2013-05
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