Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation-Reference-Cited by-同舟云学术

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Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation

Published:2014-11-13 Issue:1 Volume:60 Page:17-25
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Simioni Milena,Araujo Tânia Kawasaki,Monlleo Isabella Lopes,Maurer-Morelli Cláudia Vianna,Gil-da-Silva-Lopes Vera Lúcia

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201496.pdf

Reference63 articles.

1. Marazita, M. L . The evolution of human genetic studies of cleft lip and cleft palate. Annu. Rev. Genomics. Hum. Genet. 13, 263–283 (2012).

2. IPDTOC Working Group Prevalence at birth of cleft lip with or without cleft palate: data from the International Perinatal Database of TypicalOral Clefts (IPDTOC). Cleft Palate Cranio. J. 48, 66–81 (2011).

3. Tanaka, S. A ., Mahabir, R. C ., Jupiter, D. C ., Menezes, J. M . Updating the epidemiology of isolated cleft palate. Plast. Reconstr. Surg. 131, 650e–652e (2013).

4. Rittler, M ., Cosentino, V ., López-Camelo, J. S ., Murray, J. C ., Wehby, G ., Castilla, E. E . Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up. Am. J. Med. Genet. A 155A, 1588–1596 (2011).

5. Marazita, M. L ., Mooney, M. P . Current concepts in the embryology and genetics of cleft lip and cleft palate. Clin. Plastic. Surg. 31, 125–140 (2004).

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1. Identification of copy neutral loss of heterozygosity on chromosomes 1p, 1q, and 6p among nonsyndromic cleft lip and/or without cleft palate with hypodontia;BMC Oral Health;2023-11-29

2. Dental anomalies and their therapeutic implications: retrospective assessment of a frequent finding in patients with cleft lip and palate;BMC Oral Health;2022-12-01

3. Demographic history differences between Hispanics and Brazilians imprint haplotype features;G3 Genes|Genomes|Genetics;2022-05-02

4. Genetic and epigenetic studies in non‐syndromic oral clefts;Oral Diseases;2022-02-27

5. Clinical evaluation of patients with a neuropsychiatric risk copy number variant;Current Opinion in Genetics & Development;2021-06

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