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G Brunner

Showing results (291-300 of 727) with videos related to

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Anticancer Research|September 1, 1996
Inhibition of glycosylphosphatidylinositol (GPI) phospholipase D by suramin-like compoundsG Brunner, L Zalkow, E Burgess, et al.
American Journal of Medical Genetics|March 1, 1992
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalisB A Semmekrot, A Haraldsson, C M Weemaes, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A new web-based data mining tool for the identification of candidate genes for human genetic disordersMarc A van Driel, Koen Cuelenaere, Patrick P C W Kemmeren, et al.
Zeitschrift Fur Kardiologie|January 1, 1991
[The concept of "silent" heart failure]J Dusleag, W Klein, B Eber, et al.
Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
The Journal of Pediatrics|December 10, 1999
Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expressionI van der Burgt, G Thoonen, N Roosenboom, et al.
International Journal of Pediatric Otorhinolaryngology|June 1, 1995
Gene linkage and genetic deafnessC W Cremers, S D Brown, K P Steel, et al.
American Journal of Medical Genetics|June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spotsH G Brunner, T Hulsebos, P M Steijlen, et al.
Neuropediatrics|April 1, 1996
Association of congenital muscular dystrophy with hypoplasia of the lateral abdominal wall musculature and hypoplasia of the external genitaliaQ H Leyten, W O Renier, F J Gabreëls, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Pageof 73

Showing results (291-300 of 727) with videos related to

Sort By:
Pageof 73
Anticancer Research|September 1, 1996
Inhibition of glycosylphosphatidylinositol (GPI) phospholipase D by suramin-like compoundsG Brunner, L Zalkow, E Burgess, et al.
American Journal of Medical Genetics|March 1, 1992
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalisB A Semmekrot, A Haraldsson, C M Weemaes, et al.
European Journal of Human Genetics : EJHG|January 17, 2003
A new web-based data mining tool for the identification of candidate genes for human genetic disordersMarc A van Driel, Koen Cuelenaere, Patrick P C W Kemmeren, et al.
Zeitschrift Fur Kardiologie|January 1, 1991
[The concept of "silent" heart failure]J Dusleag, W Klein, B Eber, et al.
Neurology|January 1, 1991
Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathyH G Brunner, F Spaans, H J Smeets, et al.
The Journal of Pediatrics|December 10, 1999
Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expressionI van der Burgt, G Thoonen, N Roosenboom, et al.
International Journal of Pediatric Otorhinolaryngology|June 1, 1995
Gene linkage and genetic deafnessC W Cremers, S D Brown, K P Steel, et al.
American Journal of Medical Genetics|June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spotsH G Brunner, T Hulsebos, P M Steijlen, et al.
Neuropediatrics|April 1, 1996
Association of congenital muscular dystrophy with hypoplasia of the lateral abdominal wall musculature and hypoplasia of the external genitaliaQ H Leyten, W O Renier, F J Gabreëls, et al.
Journal of Medical Genetics|November 1, 1992
Presymptomatic diagnosis of myotonic dystrophyH G Brunner, W Nillesen, B A van Oost, et al.
Pageof 73