Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes.

Michielse, Caroline B; Bhat, Meena; Brady, Angela; Jafrid, Hussain; van den Hurk, José A J M; Raashid, Yasmin; Brunner, Han G; van Bokhoven, Hans; Padberg, George W

Michielse, Caroline B; Bhat, Meena; Brady, Angela; Jafrid, Hussain; van den Hurk, José A J M; Raashid, Yasmin; Brunner, Han G; van Bokhoven, Hans; Padberg, George W.

Affiliation

Michielse CB; Department of Neurology, University Medical Centre Nijmegen, 6500 HB Nijmegen, The Netherlands.

Eur J Hum Genet ; 14(12): 1306-12, 2006 Dec.

Article in En | MEDLINE | ID: mdl-16912702

Subject(s)

Chromosome Mapping; Chromosomes, Human, Pair 3/genetics; Facial Paralysis/genetics; Genes, Dominant/genetics; DNA Mutational Analysis; Embryonic Development/genetics; Female; Genetic Heterogeneity; Genetic Markers; Haplotypes; Heterozygote; Humans; Male; Pedigree

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 3 / Chromosome Mapping / Facial Paralysis / Genes, Dominant Type of study: Diagnostic_studies / Screening_studies Limits: Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2006 Type: Article Affiliation country: Netherlands

Search on Google

XML

PubMed Links