Interstitial deletion 4q32-34 with ulnar deficiency: 4q33 may be the critical region in 4q terminal deletion syndrome

American Journal of Medical Genetics

Volumn 99, Issue 2, 2001, Pages 94-98

  Keeling, S L ^a   Lee Jones, L ^b   Thompson, P ^b  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

4q; Chromosome deletion; Cleft lip; Cleft palate; Ulnar ray defect

Indexed keywords

ARTICLE; CARPAL BONE; CASE REPORT; CENTRAL NERVOUS SYSTEM; CHILD; CHROMOSOME 4Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION 4; CLEFT LIP; CLEFT PALATE; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DIAGNOSTIC IMAGING; DIAGNOSTIC PROCEDURE; DISEASE COURSE; HUMAN; LIMB DEVELOPMENT; MALE; METACARPAL BONE; NERVE MALFORMATION; NERVOUS SYSTEM DEVELOPMENT; PHALANX; PHENOTYPE; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; SKELETON MALFORMATION; ULNA; ULNAR NERVE;

CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; HUMANS; INFANT; MALE; SYNDROME; ULNA;

EID: 0035281584     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(2000)9999:999<00::AID-AJMG1134>3.0.CO;2-D     Document Type: Article

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