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British Medical Bulletin
|
June 15, 1999
Screening for cystic fibrosis and its evaluation
M F Wildhagen, L P ten Kate, J D Habbema
Prenatal Diagnosis
|
June 1, 1996
Down syndrome in the family: what to do when the karyotype of the proband is not available
J H Tuerlings, J C Oosterwijk, L P ten Kate
American Journal of Medical Genetics
|
August 1, 1983
Serum creatine-kinase (CK) in normal pregnancy
L P ten Kate, P J Offringa, F R Hindriks
Humangenetik
|
January 1, 1971
Fibroblast culture in Werner's syndrome
A J Nienhaus, B de Jong, L P ten Kate
Nederlands Tijdschrift Voor Geneeskunde
|
May 18, 1996
[Hereditary diseases are family diseases]
L P ten Kate, J M Collée, H G de Vries
American Journal of Medical Genetics
|
February 1, 1992
Comparison of couples referred and not referred for genetic counseling in a genetic clinic after the birth of a child with a congenital anomaly: a study in a population in the northeastern Netherlands
M C Cornel, A J van Essen, L P ten Kate
The International Journal of Risk & Safety in Medicine
|
March 21, 2013
Monitoring of risk factor/outcome combinations: a valuable supplement to birth defect monitoring
L P Ten Kate, M C Cornel, H E de Walle
Human Genetics
|
March 1, 1987
Ascertainment bias and power of procedures to estimate differences between male and female mutation rates
G J te Meerman, E R Karel, L P ten Kate
American Journal of Medical Genetics
|
January 1, 1989
Effectiveness of prevention of cystic fibrosis by artificial insemination by donor can be markedly improved by DNA-analysis of sperm donors
L P ten Kate, G J te Meerman, C H Buys
American Journal of Medical Genetics
|
November 1, 1984
Risk of Down's syndrome among second- and third-degree relatives of a proband with trisomy 21
L P ten Kate, G J te Meerman, G J Anders
Page
of 13
Search research articles
Search
Showing results (31-40 of 130) with videos related to
Sort By:
Page
of 13
British Medical Bulletin
|
June 15, 1999
Screening for cystic fibrosis and its evaluation
M F Wildhagen, L P ten Kate, J D Habbema
Prenatal Diagnosis
|
June 1, 1996
Down syndrome in the family: what to do when the karyotype of the proband is not available
J H Tuerlings, J C Oosterwijk, L P ten Kate
American Journal of Medical Genetics
|
August 1, 1983
Serum creatine-kinase (CK) in normal pregnancy
L P ten Kate, P J Offringa, F R Hindriks
Humangenetik
|
January 1, 1971
Fibroblast culture in Werner's syndrome
A J Nienhaus, B de Jong, L P ten Kate
Nederlands Tijdschrift Voor Geneeskunde
|
May 18, 1996
[Hereditary diseases are family diseases]
L P ten Kate, J M Collée, H G de Vries
American Journal of Medical Genetics
|
February 1, 1992
Comparison of couples referred and not referred for genetic counseling in a genetic clinic after the birth of a child with a congenital anomaly: a study in a population in the northeastern Netherlands
M C Cornel, A J van Essen, L P ten Kate
The International Journal of Risk & Safety in Medicine
|
March 21, 2013
Monitoring of risk factor/outcome combinations: a valuable supplement to birth defect monitoring
L P Ten Kate, M C Cornel, H E de Walle
Human Genetics
|
March 1, 1987
Ascertainment bias and power of procedures to estimate differences between male and female mutation rates
G J te Meerman, E R Karel, L P ten Kate
American Journal of Medical Genetics
|
January 1, 1989
Effectiveness of prevention of cystic fibrosis by artificial insemination by donor can be markedly improved by DNA-analysis of sperm donors
L P ten Kate, G J te Meerman, C H Buys
American Journal of Medical Genetics
|
November 1, 1984
Risk of Down's syndrome among second- and third-degree relatives of a proband with trisomy 21
L P ten Kate, G J te Meerman, G J Anders
Page
of 13