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H G Brunner

Showing results (1-10 of 179) with videos related to

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Annals of Medicine|August 1, 1995
Monoamine oxidase and behaviourH G Brunner
Ciba Foundation Symposium|January 1, 1996
MAOA deficiency and abnormal behaviour: perspectives on an associationH G Brunner
Clinical Genetics|January 6, 2007
The modular nature of genetic diseasesM Oti, H G Brunner
The New England Journal of Medicine|December 2, 1999
Precocious puberty in boysH G Brunner, B J Otten
Journal of Medical Genetics|June 1, 1991
Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresiaH G Brunner, R M Winter
Clinical Dysmorphology|October 1, 1995
Nevo syndromeB G Hilderink, H G Brunner
European Journal of Endocrinology|May 1, 1996
Luteinizing hormone receptor mutations and sex differentiationA P Themmen, H G Brunner
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 17, 1999
Testing for inherited susceptibility to breast and ovarian cancerH G Brunner, M J Ligtenberg
European Journal of Pediatrics|November 1, 1992
Craniofrontonasal dysplasiaL Kapusta, H G Brunner, B C Hamel
American Journal of Medical Genetics|June 13, 1997
Ectodermal dysplasia, cleft lip/palate, and severe cutaneous and osseous syndactyly in a mentally retarded girl: a new multiple malformation syndromeH P Freihofer, S Walji, H G Brunner
Pageof 18

Showing results (1-10 of 179) with videos related to

Sort By:
Pageof 18
Annals of Medicine|August 1, 1995
Monoamine oxidase and behaviourH G Brunner
Ciba Foundation Symposium|January 1, 1996
MAOA deficiency and abnormal behaviour: perspectives on an associationH G Brunner
Clinical Genetics|January 6, 2007
The modular nature of genetic diseasesM Oti, H G Brunner
The New England Journal of Medicine|December 2, 1999
Precocious puberty in boysH G Brunner, B J Otten
Journal of Medical Genetics|June 1, 1991
Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresiaH G Brunner, R M Winter
Clinical Dysmorphology|October 1, 1995
Nevo syndromeB G Hilderink, H G Brunner
European Journal of Endocrinology|May 1, 1996
Luteinizing hormone receptor mutations and sex differentiationA P Themmen, H G Brunner
European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 17, 1999
Testing for inherited susceptibility to breast and ovarian cancerH G Brunner, M J Ligtenberg
European Journal of Pediatrics|November 1, 1992
Craniofrontonasal dysplasiaL Kapusta, H G Brunner, B C Hamel
American Journal of Medical Genetics|June 13, 1997
Ectodermal dysplasia, cleft lip/palate, and severe cutaneous and osseous syndactyly in a mentally retarded girl: a new multiple malformation syndromeH P Freihofer, S Walji, H G Brunner
Pageof 18