Holoprosencephaly and limb reduction defects: A consideration of Steinfeld syndrome and related conditions

American Journal of Medical Genetics

Volumn 134 A, Issue 4, 2005, Pages 381-392

  Siebert, Joseph R ^a,b   Schoenecker, Kelly A ^b   Resta, Robert G ^c   Kapur, Raj P ^a,b  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c SWEDISH MEDICAL CENTER   (United States)

Author keywords

Phocomelia; Radial ray; VATER VACTERL association, MURCS, SHH, ZIC2

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CLINICAL FEATURE; CONGENITAL HEART DISEASE; CRANIOFACIAL MORPHOLOGY; DISEASE ASSOCIATION; FEMALE; FETUS; HOLOPROSENCEPHALY; HUMAN; LIMB DEFECT; MALE; METACARPAL BONE; PHENOTYPE; PRIORITY JOURNAL; RADIUS; RHOMBENCEPHALOSYNAPSIS; STEINFIELD SYNDROME; THUMB MALFORMATION;

ABNORMALITIES, MULTIPLE; ARM; CHROMOSOME ABERRATIONS; FATAL OUTCOME; FEMALE; FETAL DEATH; GESTATIONAL AGE; HOLOPROSENCEPHALY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; LEG; LIMB DEFORMITIES, CONGENITAL; MALE; SYNDROME;

EID: 18044386812     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30648     Document Type: Article

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