Otorhinolaryngologic manifestations of Hartsfield syndrome: Case series and review of literature
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Holoprosencephaly in an Egyptian baby with ectrodactyly-ectodermal dysplasia-cleft syndrome: a case report;Kalil;J. Med. Case Rep.,2012
2. Novel de novo heterozygous FGFR1 mutation in two siblings with hartsfield syndrome: a case of gonadal mosaicism;Dhamija;Am. J. Med. Genet. Part A,2014
3. Syndrome identification case report 119: hypertelorism associated with holoprosencephaly and ectrodactyly;Hartsfield;Clin. Dysmorphol.,1984
4. The face does predict the brain—midline facial and forebrain defects uncovered during the investigation of nasal obstruction and rhinorrhea: case report and a review of holoprosencephaly and its classifications;El-Hawrani;Int. J. Pediatr. Otorhinolaryngology,2006
5. Holoprosencephaly and ectrodactyly: report of three new patients and review of the literature;Keaton;Am. J. Med. Genet. Seminars Med. Genet.,2010
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1. Prenatal diagnosis of cleft lip and palate: a study of clinical utility;2023-03-24
2. Solitary Median Maxillary Central Incisor in Hartsfield Syndrome: A Case Report;International Journal of Clinical Pediatric Dentistry;2023-03-21
3. The clinical utility of genetic technologies in prenatally diagnosed cleft lip and or palate – a cohort study;2023-01-16
4. Bmp5 Mutation Alters mRNA Expression During External Ear Development;Journal of Craniofacial Surgery;2022-09-27
5. Novel synonymous and missense variants in FGFR1 causing Hartsfield syndrome;American Journal of Medical Genetics Part A;2019-09-11
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