Search research articles
Contact Us
Filters
Showing results (51-60 of 77) with videos related to
Page
of 8
Sort By:
Journal of Epidemiology and Community Health
|
September 1, 1988
Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982
L P Ten Kate, H Dolk, M C Cornel, et al.
Human Genetics
|
January 1, 1990
Chromosomal damage in peripheral blood lymphocytes of patients treated for testicular cancer
E van den Berg-de Ruiter, B de Jong, N H Mulder, et al.
Tropical Medicine & International Health : TM & IH
|
July 27, 2001
Susceptibility to development of Mycobacterium ulcerans disease: review of possible risk factors
Y Stienstra, W T van der Graaf, G J te Meerman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
July 14, 1990
[Indications for an increased risk of neural tube defects in pregnancies following ovulation induction and (or) in-vitro fertilization]
M C Cornel, L T de Jong-van den Berg, J Koudstaal, et al.
Fertility and Sterility
|
May 20, 1998
Mutation frequency of cystic fibrosis transmembrane regulator is not increased in oligozoospermic male candidates for intracytoplasmic sperm injection
J H Tuerlings, B Mol, J A Kremer, et al.
Cancer Research
|
February 1, 1989
Chromosomal changes in mature residual teratomas following polychemotherapy
S M Castedo, B de Jong, J W Oosterhuis, et al.
Cancer Genetics and Cytogenetics
|
October 1, 1993
Cytogenetic abnormalities and clinical stage in testicular nonseminomatous germ cell tumors
W E de Graaff, J van Echten-Arends, J W Oosterhuis, et al.
Human Genetics
|
September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations
H G de Vries, M A van der Meulen, R Rozen, et al.
American Journal of Human Genetics
|
August 1, 1989
Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene
H Scheffer, G J te Meerman, Y C Kruize, et al.
Journal of Medical Genetics
|
August 3, 2005
Analysis of the entire HLA region in susceptibility for cervical cancer: a comprehensive study
M Zoodsma, I M Nolte, M Schipper, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
Journal of Epidemiology and Community Health
|
September 1, 1988
Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982
L P Ten Kate, H Dolk, M C Cornel, et al.
Human Genetics
|
January 1, 1990
Chromosomal damage in peripheral blood lymphocytes of patients treated for testicular cancer
E van den Berg-de Ruiter, B de Jong, N H Mulder, et al.
Tropical Medicine & International Health : TM & IH
|
July 27, 2001
Susceptibility to development of Mycobacterium ulcerans disease: review of possible risk factors
Y Stienstra, W T van der Graaf, G J te Meerman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
July 14, 1990
[Indications for an increased risk of neural tube defects in pregnancies following ovulation induction and (or) in-vitro fertilization]
M C Cornel, L T de Jong-van den Berg, J Koudstaal, et al.
Fertility and Sterility
|
May 20, 1998
Mutation frequency of cystic fibrosis transmembrane regulator is not increased in oligozoospermic male candidates for intracytoplasmic sperm injection
J H Tuerlings, B Mol, J A Kremer, et al.
Cancer Research
|
February 1, 1989
Chromosomal changes in mature residual teratomas following polychemotherapy
S M Castedo, B de Jong, J W Oosterhuis, et al.
Cancer Genetics and Cytogenetics
|
October 1, 1993
Cytogenetic abnormalities and clinical stage in testicular nonseminomatous germ cell tumors
W E de Graaff, J van Echten-Arends, J W Oosterhuis, et al.
Human Genetics
|
September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations
H G de Vries, M A van der Meulen, R Rozen, et al.
American Journal of Human Genetics
|
August 1, 1989
Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene
H Scheffer, G J te Meerman, Y C Kruize, et al.
Journal of Medical Genetics
|
August 3, 2005
Analysis of the entire HLA region in susceptibility for cervical cancer: a comprehensive study
M Zoodsma, I M Nolte, M Schipper, et al.
Page
of 8