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H G Brunner

Showing results (11-20 of 179) with videos related to

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The Laryngoscope|October 1, 1993
Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndromeC W Cremers, H A Marres, H G Brunner
American Journal of Medical Genetics|November 1, 1993
Two additional cases of the Ohdo blepharophimosis syndromeA Maat-Kievit, H G Brunner, P Maaswinkel-Mooij
The Journal of Endocrinology|May 1, 1997
Gonadotropin receptor mutationsA P Themmen, J W Martens, H G Brunner
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive traitR J Ensink, H G Brunner, C W Cremers
Clinical Genetics|March 1, 2005
Glyc-O-genetics of Walker-Warburg syndromeJ van Reeuwijk, H G Brunner, H van Bokhoven
Archives of Otolaryngology--Head & Neck Surgery|January 1, 1997
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndromeR J Ensink, C W Cremers, H G Brunner
Molecular and Cellular Endocrinology|January 28, 1999
Activating and inactivating mutations in LH receptorsA P Themmen, J W Martens, H G Brunner
Tijdschrift Voor Kindergeneeskunde|February 1, 1993
[The Coffin-Siris syndrome. Description of 4 patients and a literature review]A F van Heyst, L A Kollée, H G Brunner
Journal of Medical Genetics|April 14, 2006
Predicting disease genes using protein-protein interactionsM Oti, B Snel, M A Huynen, et al.
Journal of Medical Genetics|June 19, 2002
The p63 gene in EEC and other syndromesH G Brunner, B C J Hamel, H Van Bokhoven
Pageof 18

Showing results (11-20 of 179) with videos related to

Sort By:
Pageof 18
The Laryngoscope|October 1, 1993
Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndromeC W Cremers, H A Marres, H G Brunner
American Journal of Medical Genetics|November 1, 1993
Two additional cases of the Ohdo blepharophimosis syndromeA Maat-Kievit, H G Brunner, P Maaswinkel-Mooij
The Journal of Endocrinology|May 1, 1997
Gonadotropin receptor mutationsA P Themmen, J W Martens, H G Brunner
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive traitR J Ensink, H G Brunner, C W Cremers
Clinical Genetics|March 1, 2005
Glyc-O-genetics of Walker-Warburg syndromeJ van Reeuwijk, H G Brunner, H van Bokhoven
Archives of Otolaryngology--Head & Neck Surgery|January 1, 1997
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndromeR J Ensink, C W Cremers, H G Brunner
Molecular and Cellular Endocrinology|January 28, 1999
Activating and inactivating mutations in LH receptorsA P Themmen, J W Martens, H G Brunner
Tijdschrift Voor Kindergeneeskunde|February 1, 1993
[The Coffin-Siris syndrome. Description of 4 patients and a literature review]A F van Heyst, L A Kollée, H G Brunner
Journal of Medical Genetics|April 14, 2006
Predicting disease genes using protein-protein interactionsM Oti, B Snel, M A Huynen, et al.
Journal of Medical Genetics|June 19, 2002
The p63 gene in EEC and other syndromesH G Brunner, B C J Hamel, H Van Bokhoven
Pageof 18