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Volumn 1, Issue 5, 2011, Pages 262-271

Refinement of the region for split hand/foot malformation 5 on 2q31.1

(36)  Theisen, A a   Rosenfeld, J A a   Shane, K b   McBride, K L b   Atkin, J F b   Gaba, C c   Hoo, J c   Kurczynski, T W d   Schnur, R E e   Coffey, L B e   Zackai, E H f   Schimmenti, L g   Friedman, N h   Zabukovec, M h   Ball, S i   Pagon, R i   Lucas, A j   Brasington, C K j   Spence, J E j   Sparks, S j   more..


Author keywords

2q31.1; DLX1 DLX2; HOXD; Limb anomalies; Microdeletion; SHFM5

Indexed keywords

ARTICLE; BRACHYDACTYLY; CHROMOSOME 2Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CORRELATION ANALYSIS; DLX1; DLX2; ECTRODACTYLY; FOOT MALFORMATION; GENE; GENOTYPE; HAND MALFORMATION; HAPLOINSUFFICIENCY; HUMAN; HYPOTHESIS; MICROARRAY ANALYSIS; PHENOTYPE; PHYSICAL DISABILITY; PRIORITY JOURNAL; SYNDACTYLY;

EID: 79957464950     PISSN: 16618769     EISSN: 16618777     Source Type: Journal    
DOI: 10.1159/000328405     Document Type: Article
Times cited : (15)

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