Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS).
Hum Genet
; 95(5): 594-5, 1995 May.
Article
em En
| MEDLINE
| ID: mdl-7759088
ABSTRACT
A TaqI RFLP was detected within the ClCN4 gene, which lies between the loci for OA1 and MLS. There were no observed recombinations between this RFLP and the OA1 mutation in three informative families. Thus, the marker will be useful for genetic counseling in OA1.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Dermatopatias
/
Cromossomo X
/
Polimorfismo de Fragmento de Restrição
/
Microftalmia
/
Albinismo Ocular
/
Ligação Genética
Limite:
Female
/
Humans
/
Male
Idioma:
En
Revista:
Hum Genet
Ano de publicação:
1995
Tipo de documento:
Article
País de afiliação:
Estados Unidos