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H G Brunner

Showing results (41-50 of 179) with videos related to

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Journal of Medical Genetics|November 1, 1992
Intestinal pseudo-obstruction in myotonic dystrophyH G Brunner, B C Hamel, P Rieu, et al.
American Journal of Medical Genetics|May 15, 1994
Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?W H Linssen, M J Van den Bent, H G Brunner, et al.
The Laryngoscope|March 16, 2000
Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutationR J Admiraal, H G Brunner, T L Dijkstra, et al.
Science (New York, N.Y.)|October 22, 1993
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase AH G Brunner, M Nelen, X O Breakefield, et al.
American Journal of Medical Genetics|April 24, 1999
Craniosynostosis associated with ectopia lentis in monozygotic twin sistersJ R Cruysberg, C M van Ravenswaaij-Arts, A Pinckers, et al.
Annales De Genetique|May 4, 2001
The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)G J Van Buggenhout, J C Trommelen, H G Brunner, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Molecular genetics of X-linked hearing impairmentH G Brunner, B Smeets, D Smeets, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumorsM J Ligtenberg, M Siers, A P Themmen, et al.
American Journal of Medical Genetics. Part A|March 29, 2005
Malpuech syndrome: three patients and a reviewW S Kerstjens-Frederikse, H G Brunner, C M L van Dael, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Biogenic amine metabolite patterns in the urine of monoamine oxidase A-deficient patients. A possible tool for diagnosisN G Abeling, A H van Gennip, H Overmars, et al.
Pageof 18

Showing results (41-50 of 179) with videos related to

Sort By:
Pageof 18
Journal of Medical Genetics|November 1, 1992
Intestinal pseudo-obstruction in myotonic dystrophyH G Brunner, B C Hamel, P Rieu, et al.
American Journal of Medical Genetics|May 15, 1994
Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?W H Linssen, M J Van den Bent, H G Brunner, et al.
The Laryngoscope|March 16, 2000
Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutationR J Admiraal, H G Brunner, T L Dijkstra, et al.
Science (New York, N.Y.)|October 22, 1993
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase AH G Brunner, M Nelen, X O Breakefield, et al.
American Journal of Medical Genetics|April 24, 1999
Craniosynostosis associated with ectopia lentis in monozygotic twin sistersJ R Cruysberg, C M van Ravenswaaij-Arts, A Pinckers, et al.
Annales De Genetique|May 4, 2001
The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)G J Van Buggenhout, J C Trommelen, H G Brunner, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Molecular genetics of X-linked hearing impairmentH G Brunner, B Smeets, D Smeets, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 1999
Analysis of mutations in genes of the follicle-stimulating hormone receptor signaling pathway in ovarian granulosa cell tumorsM J Ligtenberg, M Siers, A P Themmen, et al.
American Journal of Medical Genetics. Part A|March 29, 2005
Malpuech syndrome: three patients and a reviewW S Kerstjens-Frederikse, H G Brunner, C M L van Dael, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Biogenic amine metabolite patterns in the urine of monoamine oxidase A-deficient patients. A possible tool for diagnosisN G Abeling, A H van Gennip, H Overmars, et al.
Pageof 18