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Nederlands Tijdschrift Voor Geneeskunde
|
May 25, 1991
[Hereditary aspects of colon and rectum carcinoma; risk assessment for relatives of patients and advice for screening]
F H Menko
Disease Markers
|
December 14, 1999
Familial breast cancer: clinical services in The Netherlands
F H Menko
Human Genetics
|
April 1, 1992
Intrachromosomal insertions: a case report and a review
K Madan, F H Menko
Journal of Medical Genetics
|
September 1, 1992
Williams syndrome and chromosome 18
F H Menko, P J Stouthart
Nederlands Tijdschrift Voor Geneeskunde
|
December 28, 1999
[Two patients with Muir-Torre syndrome]
M H Vermeer, H Neering, F H Menko
Nederlands Tijdschrift Voor Geneeskunde
|
January 8, 1994
[Familial ovarian carcinoma]
R H Verheijen, F H Menko, P Kenemans
Nederlands Tijdschrift Voor Geneeskunde
|
June 29, 1996
[Hereditary mutations in the p53 tumor suppressor gene; significance for clinical practice. National Work Group Hereditary Mamma Carcinoma]
F H Menko, M A Nooy, H F Vasen
Gastroenterology
|
March 1, 1993
Variable age of onset in hereditary nonpolyposis colorectal cancer: clinical implications
F H Menko, G J te Meerman, J R Sampson
American Journal of Medical Genetics
|
November 15, 1992
Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qter
F H Menko, K Madan, J A Baart, et al.
TVZ : Het Vakblad Voor De Verpleging
|
September 1, 1988
[Education for oncological patients in the outpatient service. I. Role of the nurse]
A P Visser, F H Menko, C Breehorst, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 81) with videos related to
Sort By:
Page
of 9
Nederlands Tijdschrift Voor Geneeskunde
|
May 25, 1991
[Hereditary aspects of colon and rectum carcinoma; risk assessment for relatives of patients and advice for screening]
F H Menko
Disease Markers
|
December 14, 1999
Familial breast cancer: clinical services in The Netherlands
F H Menko
Human Genetics
|
April 1, 1992
Intrachromosomal insertions: a case report and a review
K Madan, F H Menko
Journal of Medical Genetics
|
September 1, 1992
Williams syndrome and chromosome 18
F H Menko, P J Stouthart
Nederlands Tijdschrift Voor Geneeskunde
|
December 28, 1999
[Two patients with Muir-Torre syndrome]
M H Vermeer, H Neering, F H Menko
Nederlands Tijdschrift Voor Geneeskunde
|
January 8, 1994
[Familial ovarian carcinoma]
R H Verheijen, F H Menko, P Kenemans
Nederlands Tijdschrift Voor Geneeskunde
|
June 29, 1996
[Hereditary mutations in the p53 tumor suppressor gene; significance for clinical practice. National Work Group Hereditary Mamma Carcinoma]
F H Menko, M A Nooy, H F Vasen
Gastroenterology
|
March 1, 1993
Variable age of onset in hereditary nonpolyposis colorectal cancer: clinical implications
F H Menko, G J te Meerman, J R Sampson
American Journal of Medical Genetics
|
November 15, 1992
Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qter
F H Menko, K Madan, J A Baart, et al.
TVZ : Het Vakblad Voor De Verpleging
|
September 1, 1988
[Education for oncological patients in the outpatient service. I. Role of the nurse]
A P Visser, F H Menko, C Breehorst, et al.
Page
of 9