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Results 1 - 4 of 4 for Split "hand-foot" malformation 3
  1. Chromosome 17 
    ... distinct because it does not include lissencephaly. 17p13.3 duplication syndrome, also called split-hand/foot malformation with long bone deficiency or SHFLD3, is a ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  2. TP63 gene 
    ... competing protein Tests of TP63 PubMed ADULT SYNDROME SPLIT-HAND/FOOT MALFORMATION 4; SHFM4 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3 TUMOR PROTEIN p63; TP63 LIMB-MAMMARY SYNDROME; ...
    https://medlineplus.gov/genetics/gene/tp63 - Genetics
  3. FGFR1 gene 
    ... brain development called holoprosencephaly. They also have a malformation of the hands and feet called split hand/foot. Some of these variants affect one of the ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  4. Hartsfield syndrome 
    ... condition. Hartsfield-Bixler-Demyer syndrome HHES Holoprosencephaly and split ... Dhamija R, Babovic-Vuksanovic D. FGFR1-Related Hartsfield Syndrome. 2016 Mar 3 [updated 2022 May 12]. In: Adam MP, Feldman ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics