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Journal of Medical Genetics
|
November 14, 1997
The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol
A J van Essen, A L Kneppers, A H van der Hout, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
September 28, 2001
Survival analysis in familial ovarian cancer, a case control study
R P Zweemer, R H Verheijen, J W Coebergh, et al.
American Journal of Medical Genetics
|
September 15, 1993
Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]
R H Sijmons, B Leegte, R A van Lingen, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Prenatal prediction of spinal muscular atrophy. Experience with linkage studies and consequences of present SMN deletion analysis
J M Cobben, H Scheffer, M De Visser, et al.
Prenatal Diagnosis
|
April 1, 1996
Early prenatal diagnosis of Fanconi anaemia in a twin pregnancy, using DNA analysis
M L Kwee, J R Lo Ten Foe, F Arwert, et al.
DNA and Cell Biology
|
January 1, 1997
Human uteroglobin gene: structure, subchromosomal localization, and polymorphism
Z Zhang, D B Zimonjic, N C Popescu, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2002
A genome-wide scan for preeclampsia in the Netherlands
A M Lachmeijer, R Arngrímsson, E J Bastiaans, et al.
Journal of Inherited Metabolic Disease
|
January 12, 2008
Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency
T G J Derks, T S Boer, A van Assen, et al.
BMC Medical Genetics
|
July 20, 2015
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
W Kelmemi, M E Teeuw, Z Bochdanovits, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome
J Kohlhase, P E Taschner, P Burfeind, et al.
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of 13
Search research articles
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Showing results (121-130 of 130) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 130 results.
Journal of Medical Genetics
|
November 14, 1997
The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol
A J van Essen, A L Kneppers, A H van der Hout, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology
|
September 28, 2001
Survival analysis in familial ovarian cancer, a case control study
R P Zweemer, R H Verheijen, J W Coebergh, et al.
American Journal of Medical Genetics
|
September 15, 1993
Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]
R H Sijmons, B Leegte, R A van Lingen, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1996
Prenatal prediction of spinal muscular atrophy. Experience with linkage studies and consequences of present SMN deletion analysis
J M Cobben, H Scheffer, M De Visser, et al.
Prenatal Diagnosis
|
April 1, 1996
Early prenatal diagnosis of Fanconi anaemia in a twin pregnancy, using DNA analysis
M L Kwee, J R Lo Ten Foe, F Arwert, et al.
DNA and Cell Biology
|
January 1, 1997
Human uteroglobin gene: structure, subchromosomal localization, and polymorphism
Z Zhang, D B Zimonjic, N C Popescu, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2002
A genome-wide scan for preeclampsia in the Netherlands
A M Lachmeijer, R Arngrímsson, E J Bastiaans, et al.
Journal of Inherited Metabolic Disease
|
January 12, 2008
Neonatal screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in The Netherlands: the importance of enzyme analysis to ascertain true MCAD deficiency
T G J Derks, T S Boer, A van Assen, et al.
BMC Medical Genetics
|
July 20, 2015
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
W Kelmemi, M E Teeuw, Z Bochdanovits, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome
J Kohlhase, P E Taschner, P Burfeind, et al.
Page
of 13