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06/2010
Split-hand/split-foot malformation is a rare limb malformation with median clefts of the hands and feet and aplasia/hypoplasia of the phalanges, metacarpals... 
Autosomal recessive | split-hand/split-foot malformation | syndactyly
Web Resource
Genetics and Molecular Biology, ISSN 1415-4757, 01/2018, Volume 41, Issue 1, pp. 1 - 8
Split-hand/split-foot malformation (SHFM), also known as ectrodactyly is a rare genetic disorder. It is a clinically and genetically heterogeneous group of... 
WNT10B gene | Sequence variants | Split-hand-foot malformation 6 | DEFECTS | SHFM3 | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHENOTYPE | LOCUS | HAND | DELETION | Split-Hand-Foot Malformation 6 | CONSANGUINEOUS FAMILIES | GENETICS & HEREDITY | HAND/SPLIT-FOOT MALFORMATION | sequence variants | INHERITANCE | NONSENSE MUTATION | Human and Medical Genetics
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 08/2017, Volume 34, Issue 4, pp. 476 - 480
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 9, pp. 1105 - 1110
Journal Article
Annals of Clinical and Laboratory Science, ISSN 0091-7370, 11/2017, Volume 47, Issue 6, pp. 754 - 757
Journal Article
Journal Article
American Journal of Medical Genetics, Part A, ISSN 1552-4825, 2012, Volume 158, Issue 12, pp. 3201 - 3206
  Split-hand/split-foot malformation (SHFM1) has been reported to be caused by deletions, duplications or rearrangements involving the 7q21.3 region harboring... 
Syndactyly | DLX5 and DLX6 | Split-hand/split-foot malformation 1 (SHFM1) | 7q21.3 duplication | Genetic research | Fluorescence | Cytogenetics | Medical colleges | Analysis | Genes | Finger
Journal Article