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H G Brunner

Showing results (51-60 of 179) with videos related to

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Journal of Neural Transmission. Supplementum|June 13, 1998
Monoamine oxidase A deficiency: biogenic amine metabolites in random urine samplesN G Abeling, A H van Gennip, A G van Cruchten, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14B H W Faas, J Van Der Deure, M I Wunderink, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Hearing impairment in Stickler syndromeR J C Admiraal, Y M Szymko, A J Griffith, et al.
Muscle & Nerve|March 1, 1992
Eye movement disorder: an early expression of the myotonic dystrophy gene?J P ter Bruggen, C C Tijssen, H G Brunner, et al.
Psychopathology|November 27, 2009
Psychiatric profile in rubinstein-taybi syndrome. A review and case reportW M A Verhoeven, S Tuinier, H J H Kuijpers, et al.
Journal of Medical Genetics|October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomaliesH E Cunliffe, L A McNoe, T A Ward, 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.
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.
Pageof 18

Showing results (51-60 of 179) with videos related to

Sort By:
Pageof 18
Journal of Neural Transmission. Supplementum|June 13, 1998
Monoamine oxidase A deficiency: biogenic amine metabolites in random urine samplesN G Abeling, A H van Gennip, A G van Cruchten, et al.
Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Multiple congenital abnormalities in a newborn with two supernumerary marker chromosomes derived from chromosome 14B H W Faas, J Van Der Deure, M I Wunderink, et al.
Advances in Oto-Rhino-Laryngology|November 1, 2002
Hearing impairment in Stickler syndromeR J C Admiraal, Y M Szymko, A J Griffith, et al.
Muscle & Nerve|March 1, 1992
Eye movement disorder: an early expression of the myotonic dystrophy gene?J P ter Bruggen, C C Tijssen, H G Brunner, et al.
Psychopathology|November 27, 2009
Psychiatric profile in rubinstein-taybi syndrome. A review and case reportW M A Verhoeven, S Tuinier, H J H Kuijpers, et al.
Journal of Medical Genetics|October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomaliesH E Cunliffe, L A McNoe, T A Ward, 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.
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.
Pageof 18