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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Upload12q21 deletion syndrome: Narrowing the critical region down to 1.6 Mb including SYT1 and PPP1R12A
Download from api.wiley.comExome sequencing identifies the first genetic determinants of sirenomelia in humans
UploadPrenatal findings in 1p36 deletion syndrome: New cases and a literature review
UploadRSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6
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