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Sindrome tricorrinofalangico tipo I. / Tricho-rhino-phalangeal syndrome, type 1
Bol. méd. Hosp. Infant. Méx ; 39(3): 211-4, 1982.
Article in Es | LILACS | ID: lil-9234
Responsible library: BR1.1
RESUMEN
Se presentan dos pacientes, madre e hija, con las caracteristicas clinicas y radiologicas del sindrome tricorrinofalangico tipo I. La enfermedad sigue herencia autosomica dominante y tiene expresividad variable. Se senala el diagnostico diferencial con el sindrome tricorrinofalangico tipo II
Subject(s)
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Collection: 01-internacional Database: LILACS Main subject: Abnormalities, Multiple Limits: Adolescent / Female / Humans Language: Es Journal: Bol. méd. Hosp. Infant. Méx Journal subject: PEDIATRIA Year: 1982 Document type: Article Country of publication: Mexico
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Collection: 01-internacional Database: LILACS Main subject: Abnormalities, Multiple Limits: Adolescent / Female / Humans Language: Es Journal: Bol. méd. Hosp. Infant. Méx Journal subject: PEDIATRIA Year: 1982 Document type: Article Country of publication: Mexico