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The Laryngoscope
|
October 1, 1993
Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndrome
C W Cremers, H A Marres, H G Brunner
American Journal of Medical Genetics
|
November 1, 1993
Two additional cases of the Ohdo blepharophimosis syndrome
A Maat-Kievit, H G Brunner, P Maaswinkel-Mooij
The Journal of Endocrinology
|
May 1, 1997
Gonadotropin receptor mutations
A 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 trait
R J Ensink, H G Brunner, C W Cremers
Clinical Genetics
|
March 1, 2005
Glyc-O-genetics of Walker-Warburg syndrome
J van Reeuwijk, H G Brunner, H van Bokhoven
Archives of Otolaryngology--Head & Neck Surgery
|
January 1, 1997
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome
R J Ensink, C W Cremers, H G Brunner
Molecular and Cellular Endocrinology
|
January 28, 1999
Activating and inactivating mutations in LH receptors
A 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 interactions
M Oti, B Snel, M A Huynen, et al.
Journal of Medical Genetics
|
June 19, 2002
The p63 gene in EEC and other syndromes
H G Brunner, B C J Hamel, H Van Bokhoven
Page
of 18
Search research articles
Search
Showing results (11-20 of 179) with videos related to
Sort By:
Page
of 18
The Laryngoscope
|
October 1, 1993
Neo-oval window technique and myringo-chorda-vestibulopexy in the BOR syndrome
C W Cremers, H A Marres, H G Brunner
American Journal of Medical Genetics
|
November 1, 1993
Two additional cases of the Ohdo blepharophimosis syndrome
A Maat-Kievit, H G Brunner, P Maaswinkel-Mooij
The Journal of Endocrinology
|
May 1, 1997
Gonadotropin receptor mutations
A 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 trait
R J Ensink, H G Brunner, C W Cremers
Clinical Genetics
|
March 1, 2005
Glyc-O-genetics of Walker-Warburg syndrome
J van Reeuwijk, H G Brunner, H van Bokhoven
Archives of Otolaryngology--Head & Neck Surgery
|
January 1, 1997
Congenital conductive hearing loss in the lacrimoauriculodentodigital syndrome
R J Ensink, C W Cremers, H G Brunner
Molecular and Cellular Endocrinology
|
January 28, 1999
Activating and inactivating mutations in LH receptors
A 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 interactions
M Oti, B Snel, M A Huynen, et al.
Journal of Medical Genetics
|
June 19, 2002
The p63 gene in EEC and other syndromes
H G Brunner, B C J Hamel, H Van Bokhoven
Page
of 18