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Nederlands Tijdschrift Voor Geneeskunde
|
April 4, 1981
[A mentally retarded male with multiple congenital anomalies, epilepsy and trisomy 9p and partial monosomy 17q]
G J van der Linden, A Dumoré-Balek, H Veenema, et al.
Experimental Cell Research
|
October 1, 1975
Polymorphisms for human chromosomes 1 and Y. Feulgen and UV DNA measurements
J P Geraedts, P L Pearson, M van der Ploeg, et al.
Immunogenetics
|
January 1, 1983
The recognition of abnormal sex chromosome constitution by HLA-restricted anti-H-Y cytotoxic T cells and antibody
E Goulmy, A van Leeuwen, E Blokland, et al.
Human Genetics
|
December 1, 1993
RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families
H Meijer, R J Jongbloed, M Hekking, et al.
Transfusion
|
May 1, 1994
A study of the prevalence and patterns of inheritance of partial D antigen category VI in a white donor population
E A Beckers, P M Thijssen, J P Geraedts, et al.
Tijdschrift Voor Kindergeneeskunde
|
February 1, 1984
[Familial mental retardation and the fragile X syndrome]
H Veenema, A J Pelckmans, J P Geraedts, et al.
Scandinavian Journal of Haematology
|
July 1, 1981
Clones with 5q - and inversion of chromosome 7 in PHA stimulated peripheral blood
C H Leeksma, J den Nijs, F Havik, et al.
Journal of Reproduction and Fertility
|
March 1, 1992
Positive effect of taurine on preimplantation development of mouse embryos in vitro
J C Dumoulin, J L Evers, M Bras, et al.
Human Reproduction (Oxford, England)
|
April 1, 1995
Application of different in-situ hybridization detection methods for human sperm analysis
E Martini, E J Speel, J P Geraedts, et al.
Brain : a Journal of Neurology
|
June 1, 1989
Anticipation in myotonic dystrophy: fact or fiction?
C J Höweler, H F Busch, J P Geraedts, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 134) with videos related to
Sort By:
Page
of 14
Nederlands Tijdschrift Voor Geneeskunde
|
April 4, 1981
[A mentally retarded male with multiple congenital anomalies, epilepsy and trisomy 9p and partial monosomy 17q]
G J van der Linden, A Dumoré-Balek, H Veenema, et al.
Experimental Cell Research
|
October 1, 1975
Polymorphisms for human chromosomes 1 and Y. Feulgen and UV DNA measurements
J P Geraedts, P L Pearson, M van der Ploeg, et al.
Immunogenetics
|
January 1, 1983
The recognition of abnormal sex chromosome constitution by HLA-restricted anti-H-Y cytotoxic T cells and antibody
E Goulmy, A van Leeuwen, E Blokland, et al.
Human Genetics
|
December 1, 1993
RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families
H Meijer, R J Jongbloed, M Hekking, et al.
Transfusion
|
May 1, 1994
A study of the prevalence and patterns of inheritance of partial D antigen category VI in a white donor population
E A Beckers, P M Thijssen, J P Geraedts, et al.
Tijdschrift Voor Kindergeneeskunde
|
February 1, 1984
[Familial mental retardation and the fragile X syndrome]
H Veenema, A J Pelckmans, J P Geraedts, et al.
Scandinavian Journal of Haematology
|
July 1, 1981
Clones with 5q - and inversion of chromosome 7 in PHA stimulated peripheral blood
C H Leeksma, J den Nijs, F Havik, et al.
Journal of Reproduction and Fertility
|
March 1, 1992
Positive effect of taurine on preimplantation development of mouse embryos in vitro
J C Dumoulin, J L Evers, M Bras, et al.
Human Reproduction (Oxford, England)
|
April 1, 1995
Application of different in-situ hybridization detection methods for human sperm analysis
E Martini, E J Speel, J P Geraedts, et al.
Brain : a Journal of Neurology
|
June 1, 1989
Anticipation in myotonic dystrophy: fact or fiction?
C J Höweler, H F Busch, J P Geraedts, et al.
Page
of 14