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B C Hamel

Showing results (61-70 of 129) with videos related to

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American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.
Clinical Dysmorphology|January 1, 1996
Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new associationJ J Van Den Ende, C J Van Der Burgt, M C Jansweijer, et al.
Human Genetics|June 1, 1995
Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyF A Hol, B C Hamel, M P Geurds, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.
American Journal of Medical Genetics|December 1, 1989
Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardationR C Hennekam, R A Geerdink, B C Hamel, et al.
American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
Journal of Medical Genetics|March 2, 1999
A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric regionB C Hamel, P Wesseling, W O Renier, et al.
Archives of Dermatology|February 1, 1992
Restrictive dermopathy in two brothersR Happle, J H Stekhoven, B C Hamel, et al.
American Journal of Medical Genetics|April 10, 1995
Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier reportB C Hamel, J M Draaisma, A J Pinckers, et al.
Neuromuscular Disorders : NMD|March 31, 2019
First familial Becker muscular dystrophy in Tanzania: Clinical and genetic features<sup>.</sup>M C J Dekker, A A Tieleman, O J Igogo, et al.
Pageof 13

Showing results (61-70 of 129) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|April 20, 1999
Psychometric assessment of families with X-linked mental retardationT van Roosmalen, A P Smits, G H Thoonen, et al.
Clinical Dysmorphology|January 1, 1996
Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new associationJ J Van Den Ende, C J Van Der Burgt, M C Jansweijer, et al.
Human Genetics|June 1, 1995
Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyF A Hol, B C Hamel, M P Geurds, et al.
American Journal of Medical Genetics|April 1, 1992
Penetrance of fra(X) gene: influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting maleA P Smits, B A van Oost, A F de Haan, et al.
American Journal of Medical Genetics|December 1, 1989
Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardationR C Hennekam, R A Geerdink, B C Hamel, et al.
American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
Journal of Medical Genetics|March 2, 1999
A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric regionB C Hamel, P Wesseling, W O Renier, et al.
Archives of Dermatology|February 1, 1992
Restrictive dermopathy in two brothersR Happle, J H Stekhoven, B C Hamel, et al.
American Journal of Medical Genetics|April 10, 1995
Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier reportB C Hamel, J M Draaisma, A J Pinckers, et al.
Neuromuscular Disorders : NMD|March 31, 2019
First familial Becker muscular dystrophy in Tanzania: Clinical and genetic features<sup>.</sup>M C J Dekker, A A Tieleman, O J Igogo, et al.
Pageof 13