A variant example of familial Floating-Harbor syndrome?

Genetic Counseling

Volumn 14, Issue 1, 2003, Pages 31-37

  Penaloza J M ^a   Garcia Cruz D ^a   Davalos I P ^a,c   Davalos N O ^a,c   Garcia Cruz M O ^d   Perez Rulfo D ^d   Sanchez Corona, J ^b  

^a CENTRO DE INVESTIGACIÓN BIOMÉDICA DE OCCIDENTE   (Mexico)

^b Division de Medicina Molecular   (Mexico)

^c UNIVERSITY OF GUADALAJARA   (Mexico)

^d INSTITUTO MEXICANO DEL SEGURO SOCIAL   (Mexico)

Author keywords

Autosomal dominant inheritance; Celiac Disease; Floating Harbor syndrome; Short stature

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BONE AGE; CASE REPORT; CELIAC DISEASE; CHILD; FAMILIAL DISEASE; FLOATING HARBOR SYNDROME; GENETIC VARIABILITY; GROWTH RETARDATION; HUMAN; MALE; MULTIGENE FAMILY; PHENOTYPE; SHORT STATURE; SPEECH DEVELOPMENT;

AGE DETERMINATION BY SKELETON; BONE DISEASES, DEVELOPMENTAL; CELIAC DISEASE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; DWARFISM; FACIES; HETEROZYGOTE DETECTION; HUMANS; LANGUAGE DEVELOPMENT DISORDERS; MALE; SYNDROME; VARIATION (GENETICS);

COLUMELLA;

EID: 0037239536     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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