Bowen-Conradi syndrome

Clinical Dysmorphology

Volumn 11, Issue 2, 2002, Pages 149-

  Lemire, Edmond G ^a  

^a ROYAL UNIVERSITY HOSPITAL   (Canada)

Author keywords

Bowen Conradi syndrome; Hutterite

Indexed keywords

BOWEN CONRADI SYNDROME; CLINICAL FEATURE; DATA BASE; ETHNIC GROUP; FAILURE TO THRIVE; FOOT MALFORMATION; HUMAN; INTRAUTERINE GROWTH RETARDATION; LETTER; MALFORMATION SYNDROME; MEDICAL LITERATURE; MICROCEPHALY; PRIORITY JOURNAL; TRISOMY 18; CONGENITAL MALFORMATION; ETHNOLOGY; GENETICS; INFANT; MICROGNATHIA; MULTIPLE MALFORMATION SYNDROME; NEWBORN; NOSE; NOTE; RECESSIVE GENE; RELIGION; SYNDROME;

ABNORMALITIES, MULTIPLE; CHRISTIANITY; ETHNIC GROUPS; FAILURE TO THRIVE; FETAL GROWTH RETARDATION; GENES, RECESSIVE; HUMANS; INFANT; INFANT, NEWBORN; MICROCEPHALY; MICROGNATHISM; NOSE; SYNDROME;

EID: 0036215023     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200204000-00018     Document Type: Letter

References (4)

1. Syndrome of skeletal and genitourinary anomalies with unusual facies and failure to thrive in hutterite sibs
2. Bowen-Conradi syndrome in an Indian infant: First non Hutterite case
3. The Bowen-Conradi syndrome - A highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight and joint deformities
4. La phénocopie de la trisomie 18: Une maladie autosomique récessive?