[Familial Pierre Robin's anomaly]. / Anomalía familiar de Pierre Robin.
Bol Med Hosp Infant Mex
; 35(6): 1155-60, 1978.
Article
em Es
| MEDLINE
| ID: mdl-687423
The present paper describes a family with daughter and son affected with clinical characteristics of Pierre Robin's anomaly. The pedigree suggests an autosomal recessive inheritance pattern. The authors mention that in order to have more genetic evidence on this trait, an extensive study of families, with at least one proband should be made for a correct genetic analysis.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Síndrome de Pierre Robin
Limite:
Child
/
Female
/
Humans
/
Male
/
Newborn
Idioma:
Es
Revista:
Bol Med Hosp Infant Mex
Ano de publicação:
1978
Tipo de documento:
Article
País de publicação:
México