Hirschsprung disease, mental retardation and dysmorphic facial features in five unrelated children

Clinical Dysmorphology

Volumn 10, Issue 3, 2001, Pages 157-163

  Kaariainen H ^a   Wallgren Pettersson, C ^b   Clarke, A ^f   Pihko, H ^c   Taskinen, H ^d,e   Rintala, R ^c  

^a Vaestoliitto   (Finland)

^b FOLKHÄLSAN RESEARCH CENTER   (Finland)

^c UNIVERSITY OF HELSINKI AND HELSINKI UNIVERSITY HOSPITAL   (Finland)

^d FINNISH INSTITUTE OF OCCUPATIONAL HEALTH   (Finland)

^e UNIVERSITY OF TAMPERE   (Finland)

^f UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

Chromosome 2q22; Dysmorphic features; Hirschsprung disease; Hypospadias; Mental retardation

Indexed keywords

ARTICLE; CHILD; CHILDHOOD DISEASE; CHROMOSOME 2Q; CLINICAL ARTICLE; CLINICAL FEATURE; FACE DYSMORPHIA; FACIES; FEMALE; GENE TRANSLOCATION; GROWTH RETARDATION; HIRSCHSPRUNG DISEASE; HUMAN; HYPERTELORISM; HYPOSPADIAS; INFANT; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; POSTNATAL GROWTH; PRIORITY JOURNAL;

EID: 0034951117     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200107000-00001     Document Type: Article

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