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Showing results (171-180 of 228) with videos related to

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Muscle & Nerve. Supplement|April 12, 2013
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.
The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.
Brain Communications|September 21, 2020
Ophthalmological findings in facioscapulohumeral dystrophyRianne J M Goselink, Vivian Schreur, Caroline R van Kernebeek, et al.
World Journal of Emergency Surgery : WJES|November 10, 2015
The impact of early surgical intervention in free intestinal perforation: a time-to-intervention pilot studyAndreas Hecker, E Schneck, R Röhrig, et al.
Neurology|September 6, 2007
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDJ C de Greef, M Wohlgemuth, O A Chan, et al.
Annals of Neurology|July 17, 1998
Genetic characteristics of myoadenylate deaminase deficiencyH T Verzijl, B G van Engelen, J A Luyten, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophyC Wijmenga, R R Frants, J E Hewitt, et al.
Transplantation Proceedings|May 28, 2005
sCD30 and neopterin as risk factors of chronic renal transplant rejection: impact of cyclosporine A, tacrolimus, and mycophenolate mofetilR Weimer, C Süsal, S Yildiz, et al.
Human Molecular Genetics|December 1, 1993
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unitJ C van Deutekom, C Wijmenga, E A van Tienhoven, et al.
Human Molecular Genetics|September 1, 1996
Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch familyH Kremer, L P Kuyt, B van den Helm, et al.
Pageof 23

Showing results (171-180 of 228) with videos related to

Sort By:
Pageof 23
Muscle & Nerve. Supplement|April 12, 2013
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.
The New England Journal of Medicine|August 18, 1994
Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two familiesP Coucke, G Van Camp, B Djoyodiharjo, et al.
Brain Communications|September 21, 2020
Ophthalmological findings in facioscapulohumeral dystrophyRianne J M Goselink, Vivian Schreur, Caroline R van Kernebeek, et al.
World Journal of Emergency Surgery : WJES|November 10, 2015
The impact of early surgical intervention in free intestinal perforation: a time-to-intervention pilot studyAndreas Hecker, E Schneck, R Röhrig, et al.
Neurology|September 6, 2007
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDJ C de Greef, M Wohlgemuth, O A Chan, et al.
Annals of Neurology|July 17, 1998
Genetic characteristics of myoadenylate deaminase deficiencyH T Verzijl, B G van Engelen, J A Luyten, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Molecular genetics of facioscapulohumeral muscular dystrophyC Wijmenga, R R Frants, J E Hewitt, et al.
Transplantation Proceedings|May 28, 2005
sCD30 and neopterin as risk factors of chronic renal transplant rejection: impact of cyclosporine A, tacrolimus, and mycophenolate mofetilR Weimer, C Süsal, S Yildiz, et al.
Human Molecular Genetics|December 1, 1993
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unitJ C van Deutekom, C Wijmenga, E A van Tienhoven, et al.
Human Molecular Genetics|September 1, 1996
Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch familyH Kremer, L P Kuyt, B van den Helm, et al.
Pageof 23