Interstitial deletion of chromosome 2p16.2p21

Clinical Dysmorphology

Volumn 12, Issue 3, 2003, Pages 183-185

  Sanders, Shannon R ^a,b   Dawson, A J ^a   Vust, A ^a   Hryshko, M ^a   Tomiuk, M ^a   Riordan, D ^a   Prasad, C ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

^b Dept of Pediatrics and Child Health   (Canada)

Author keywords

2p deletion; Development delay; Facial dysmorphism

Indexed keywords

ARTICLE; CASE REPORT; CHILD DEVELOPMENT; CHROMOSOME 2; CHROMOSOME 2P; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; CHROMOSOME BREAKAGE; CHROMOSOME DELETION 2; CHROMOSOME STRUCTURE; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; FACIES; FEMALE; GENETICS; HEART ATRIUM SEPTUM DEFECT; HUMAN; HYPOTELORISM; INFANT; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE 46,XX; PHENOTYPE; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0041866706     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200307000-00007     Document Type: Article

References (4)

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