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Y Alanay

Showing results (11-20 of 14) with videos related to

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Journal of Medical Genetics|June 11, 2009
Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseasesT Furuichi, H Kayserili, S Hiraoka, et al.
Journal of Intellectual Disability Research : JIDR|January 16, 2007
A multidisciplinary approach to the management of individuals with fragile X syndromeY Alanay, F Unal, G Turanli, et al.
Human Genetics|April 10, 2013
Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndromeJ C Czeschik, C Voigt, Y Alanay, et al.
Clinical Genetics|February 24, 2017
Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 casesE Ranza, C Huber, N Levin, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Journal of Medical Genetics|June 11, 2009
Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseasesT Furuichi, H Kayserili, S Hiraoka, et al.
Journal of Intellectual Disability Research : JIDR|January 16, 2007
A multidisciplinary approach to the management of individuals with fragile X syndromeY Alanay, F Unal, G Turanli, et al.
Human Genetics|April 10, 2013
Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndromeJ C Czeschik, C Voigt, Y Alanay, et al.
Clinical Genetics|February 24, 2017
Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 casesE Ranza, C Huber, N Levin, et al.
Pageof 2