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B A van Oost

Showing results (71-80 of 107) with videos related to

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The Journal of Clinical Investigation|September 1, 1996
Benign familial hematuria due to mutation of the type IV collagen alpha4 geneH H Lemmink, W N Nillesen, T Mochizuki, et al.
American Journal of Medical Genetics|December 1, 1992
Prenatal exclusion of choroideremiaJ A van den Hurk, P M van Zandvoort, F Brunsmann, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.
Cytogenetic and Genome Research|February 14, 2003
A radiation hybrid map of the X-chromosome of the dog (Canis familiaris)R E Everts, M E van Wolferen, S A Versteeg, et al.
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndromeD D de Vries, C J Buzing, W Ruitenbeek, et al.
Neuromuscular Disorders : NMD|September 1, 1994
The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28E A Janssen, G W Hensels, B A van Oost, et al.
The Journal of Heredity|October 12, 2004
Analysis of the inheritance of white spotting and the evaluation of KIT and EDNRB as spotting loci in Dutch boxer dogsM A E van Hagen, J van der Kolk, M A M Barendse, et al.
Archives of Neurology|April 1, 1995
Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiencyA T Hageman, F J Gabreëls, J G de Jong, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
The Journal of Clinical Investigation|September 1, 1996
Benign familial hematuria due to mutation of the type IV collagen alpha4 geneH H Lemmink, W N Nillesen, T Mochizuki, et al.
American Journal of Medical Genetics|December 1, 1992
Prenatal exclusion of choroideremiaJ A van den Hurk, P M van Zandvoort, F Brunsmann, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
Genomics|October 1, 1993
The gene for spondyloepiphyseal dysplasia (SEDL) maps to Xp22 between DXS16 and DXS92S Heuertz, M Nelen, A O Wilkie, et al.
Cytogenetic and Genome Research|February 14, 2003
A radiation hybrid map of the X-chromosome of the dog (Canis familiaris)R E Everts, M E van Wolferen, S A Versteeg, et al.
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndromeD D de Vries, C J Buzing, W Ruitenbeek, et al.
Neuromuscular Disorders : NMD|September 1, 1994
The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28E A Janssen, G W Hensels, B A van Oost, et al.
The Journal of Heredity|October 12, 2004
Analysis of the inheritance of white spotting and the evaluation of KIT and EDNRB as spotting loci in Dutch boxer dogsM A E van Hagen, J van der Kolk, M A M Barendse, et al.
Archives of Neurology|April 1, 1995
Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiencyA T Hageman, F J Gabreëls, J G de Jong, et al.
Pageof 11