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Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 2, 2009
Marfan syndrome masked by Down syndrome?
J C Vis, K van Engelen, J Timmermans, 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.
Journal of Medical Genetics
|
January 1, 1990
Oculocerebrocutaneous syndrome
L M Bleeker-Wagemakers, B C Hamel, R C Hennekam, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 8, 1997
[Ehlers-Danlos syndrome IV: phenotype variation]
C H Engels, P W van Dongen, G H Boers, et al.
Neuromuscular Disorders : NMD
|
June 26, 2007
Reduced quantitative muscle function in tenascin-X deficient Ehlers-Danlos patients
N C Voermans, T M Altenburg, B C Hamel, et al.
American Journal of Medical Genetics
|
March 4, 2000
Cri du chat syndrome: changing phenotype in older patients
G J Van Buggenhout, E Pijkels, M Holvoet, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies
N C Voermans, G J Jenniskens, B C Hamel, et al.
American Journal of Medical Genetics
|
July 15, 1994
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies
B C Hamel, E C Mariman, S E van Beersum, et al.
Tijdschrift Voor Kindergeneeskunde
|
February 1, 1985
[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?]
R C Sengers, B C Hamel, B J Otten, et al.
American Journal of Medical Genetics
|
October 6, 1999
Perlman syndrome: four additional cases and review
H T Henneveld, R A van Lingen, B C Hamel, et al.
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of 13
Search research articles
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Showing results (41-50 of 129) with videos related to
Sort By:
Page
of 13
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 2, 2009
Marfan syndrome masked by Down syndrome?
J C Vis, K van Engelen, J Timmermans, 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.
Journal of Medical Genetics
|
January 1, 1990
Oculocerebrocutaneous syndrome
L M Bleeker-Wagemakers, B C Hamel, R C Hennekam, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 8, 1997
[Ehlers-Danlos syndrome IV: phenotype variation]
C H Engels, P W van Dongen, G H Boers, et al.
Neuromuscular Disorders : NMD
|
June 26, 2007
Reduced quantitative muscle function in tenascin-X deficient Ehlers-Danlos patients
N C Voermans, T M Altenburg, B C Hamel, et al.
American Journal of Medical Genetics
|
March 4, 2000
Cri du chat syndrome: changing phenotype in older patients
G J Van Buggenhout, E Pijkels, M Holvoet, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies
N C Voermans, G J Jenniskens, B C Hamel, et al.
American Journal of Medical Genetics
|
July 15, 1994
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies
B C Hamel, E C Mariman, S E van Beersum, et al.
Tijdschrift Voor Kindergeneeskunde
|
February 1, 1985
[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?]
R C Sengers, B C Hamel, B J Otten, et al.
American Journal of Medical Genetics
|
October 6, 1999
Perlman syndrome: four additional cases and review
H T Henneveld, R A van Lingen, B C Hamel, et al.
Page
of 13