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4. Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27. Ianakiev P; Kilpatrick MW; Toudjarska I; Basel D; Beighton P; Tsipouras P Am J Hum Genet; 2000 Jul; 67(1):59-66. PubMed ID: 10839977 [TBL] [Abstract][Full Text] [Related]
5. Discrepancies in upper and lower limb patterning in split hand foot malformation. Elliott AM; Reed MH; Roscioli T; Evans JA Clin Genet; 2005 Nov; 68(5):408-23. PubMed ID: 16207208 [TBL] [Abstract][Full Text] [Related]
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12. The p63 gene in EEC and other syndromes. Brunner HG; Hamel BC; Van Bokhoven H J Med Genet; 2002 Jun; 39(6):377-81. PubMed ID: 12070241 [TBL] [Abstract][Full Text] [Related]
13. Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family. Peng Y; Yang S; Xi H; Hu J; Jia Z; Pang J; Liu J; Yu W; Tang C; Wang H Mol Genet Genomic Med; 2021 Mar; 9(3):e1604. PubMed ID: 33471964 [TBL] [Abstract][Full Text] [Related]
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15. A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation. Babbs C; Heller R; Everman DB; Crocker M; Twigg SR; Schwartz CE; Giele H; Wilkie AO Hum Genet; 2007 Sep; 122(2):191-9. PubMed ID: 17569090 [TBL] [Abstract][Full Text] [Related]
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