6 results on '"Syndactyly -- Genetic aspects"'
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2. Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani-Lenz-like non-syndromic oligosyndactyly
3. Triphalangeal thumb-polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer
4. A microduplication of the long range of SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome
5. Syndactyly type-I: study of four large Indian pedigrees
6. Mutation in the IgII domain of FGFR2 causes the eponymous form of Pfeiffer syndrome
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