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Showing results (71-80 of 75) with videos related to

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Journal of Medical Genetics|July 1, 1990
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18P Heutink, B J van de Wetering, G J Breedveld, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
Human Mutation|September 12, 2000
Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasiaK Laake, L Jansen, J M Hahnemann, et al.
Clinical Genetics|March 13, 2016
Expanding the genotypic spectrum of Perrault syndromeL A M Demain, J E Urquhart, J O'Sullivan, et al.
Human Molecular Genetics|February 13, 2001
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGHC E Bruder, C Hirvelä, I Tapia-Paez, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Journal of Medical Genetics|July 1, 1990
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18P Heutink, B J van de Wetering, G J Breedveld, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
Human Mutation|September 12, 2000
Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasiaK Laake, L Jansen, J M Hahnemann, et al.
Clinical Genetics|March 13, 2016
Expanding the genotypic spectrum of Perrault syndromeL A M Demain, J E Urquhart, J O'Sullivan, et al.
Human Molecular Genetics|February 13, 2001
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGHC E Bruder, C Hirvelä, I Tapia-Paez, et al.
Pageof 8