A case-control study of environmental exposures for nonsyndromic cleft of the lip and/or palate in eastern Guangdong, China
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference47 articles.
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3. Loss of function mutations in FGFR1 cause autosomal dominant Kallmann syndrome;Dode;Nat. Genet.,2003
4. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and anykloglossia;Braybrook;Nat. Genet.,2001
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2. Oral Cleft and Maternal History of Spontaneous Abortion: A Case-Control Study;The Cleft Palate Craniofacial Journal;2023-11-15
3. Genetic Inheritance Models of Non-Syndromic Cleft Lip with or without Palate: From Monogenic to Polygenic;Genes;2023-09-24
4. Epidemiological and Spatiotemporal Descriptive Analysis of Patients with Nonsyndromic Cleft Lip and/or Palate: A 12-Year Retrospective Study in Southern Iran;BioMed Research International;2023-04-19
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