The oculo-dento-digital syndrome: Male-to-male transmission and variable expression in a family

Genetic Counseling

Volumn 8, Issue 2, 1997, Pages 87-90

  Ioan, D M ^a   Dumitriu, L ^a   Belengeariu, V ^b   Fryns, J P ^c  

^a C I PARHON NATIONAL INSTITUTE OF ENDOCRINOLOGY   (Romania)

^b Faculty of Medicine   (Romania)

^c UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Autosomal dominant inheritance; Microphthalmos; Oculo dento digital syndrome; Syndactyly

Indexed keywords

ARTICLE; CASE REPORT; CHILD; ENAMEL HYPOPLASIA; EYE MALFORMATION; FAMILY STUDY; FEMALE; FINGER MALFORMATION; HALLERMANN STREIFF SYNDROME; HUMAN; HYPODONTIA; MALE; MALFORMATION SYNDROME; PRESCHOOL CHILD; SIBLING; SYNDACTYLY; TOOTH MALFORMATION; VERTICAL TRANSMISSION;

RAPHIA FRATER;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FACIES; FEMALE; GENE EXPRESSION; HUMANS; MALE; MICROPHTHALMOS; SYNDACTYLY; SYNDROME; TOOTH ABNORMALITIES;

EID: 0030942653     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

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