Ectropion Inferior Cleft Lip And Or Palate
Last Posted: Dec 21, 2020
- Screening of IRF6 Variants in Patients Subjected to Genetic Association Studies for Nonsyndromic Cleft Lip/Palate.
Velázquez-Aragón José A et al. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2020 Dec 1055665620980238
- International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): diagnosis, follow-up and management.
Altassan Ruqaiah et al. Journal of inherited metabolic disease 2020 Jul
- Delivering effective genetic services for patients and families affected by cleft lip and/or palate.
Stock Nicola Marie et al. European journal of human genetics : EJHG 2019 Jan
- Comprehensive Genetic Screening Recommended for Nonsyndromic Cleft Lip/Palate: Even in the absence of any signs of a syndrome, patients with cleft lip/palate may still carry a mutation in a gene linked to a syndrome and should receive comprehensive genetic testing.
et al. American journal of medical genetics. Part A 2018 Jun 176(6) 1280-1282
- Consumer DNA testing promises more than it delivers
TH Sae, Science News, May 22, 2018
- Epidemiology of orofacial clefts in a Danish county over 35 years - Before and after implementation of a prenatal screening programme for congenital anomalies.
Paaske Eva Berenth et al. European journal of medical genetics 2018 May
- Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
Basha Mirta et al. Journal of medical genetics 2018 Mar
- Development of a 22q11DS psycho-educational programme: exploration of the views, concerns and educational needs of parents caring for children or adolescents with 22q11DS in relation to mental health issues.
Alugo T et al. Child: care, health and development 2017 Mar
- Genetic Screening in Patients with Craniofacial Malformations.
Yoon Amanda J et al. Journal of pediatric genetics 2016 Dec 5(4) 220-224
- Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers.
van der Post Rachel S et al. Journal of medical genetics 2015 Jun 52(6) 361-74
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