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Birth Defects Original Article Series
|
January 1, 1991
The dermatoglyphics of nonhuman primates: a neglected resource
L Newell-Morris, T F Wienker
Journal of Medical Genetics
|
February 1, 1993
On the genetics of mandibular prognathism: analysis of large European noble families
G Wolff, T F Wienker, H Sander
American Journal of Medical Genetics
|
September 1, 1987
Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal Xq
P Wieacker, G Wolff, T F Wienker
Journal of Molecular Medicine (Berlin, Germany)
|
February 1, 1996
Role of T cell receptor delta gene in susceptibility to celiac disease
E Roschmann, T F Wienker, B A Volk
Clinical Genetics
|
June 1, 1976
Prenatal diagnosis of homoxygous familial hypercholesterolemia: investigation of a case at risk
T F Wienker, G Utermann, H H Ropers
Cancer Genetics and Cytogenetics
|
March 1, 1988
High-resolution chromosome banding and fragile site studies in von Hippel-Lindau syndrome
H P Neumann, W Schempp, T F Wienker
Deutsche Medizinische Wochenschrift (1946)
|
October 29, 1976
[Color blindness: in high school students less often than in elementary school pupils]
K Feig, T F Wienker, H H Ropers
Human Genetics
|
June 29, 1976
Fabry's disease: heterozygote detection by hair root analysis
T Grimm, T F Wienker, H H Ropers
Human Genetics
|
February 1, 1980
The presence of androgen-binding receptors in genital and nongenital skin fibroblasts
J Herfert, T F Wienker, H H Ropers
Nucleic Acids Research
|
April 25, 1989
A BAM HI RFLP at the human tyrosine aminotransferase (TAT) gene locus at 16q
B Wullich, E Natt, T F Wienker, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 104) with videos related to
Sort By:
Page
of 11
Birth Defects Original Article Series
|
January 1, 1991
The dermatoglyphics of nonhuman primates: a neglected resource
L Newell-Morris, T F Wienker
Journal of Medical Genetics
|
February 1, 1993
On the genetics of mandibular prognathism: analysis of large European noble families
G Wolff, T F Wienker, H Sander
American Journal of Medical Genetics
|
September 1, 1987
Close linkage of the Wieacker-Wolff syndrome to the DNA segment DXYS1 in proximal Xq
P Wieacker, G Wolff, T F Wienker
Journal of Molecular Medicine (Berlin, Germany)
|
February 1, 1996
Role of T cell receptor delta gene in susceptibility to celiac disease
E Roschmann, T F Wienker, B A Volk
Clinical Genetics
|
June 1, 1976
Prenatal diagnosis of homoxygous familial hypercholesterolemia: investigation of a case at risk
T F Wienker, G Utermann, H H Ropers
Cancer Genetics and Cytogenetics
|
March 1, 1988
High-resolution chromosome banding and fragile site studies in von Hippel-Lindau syndrome
H P Neumann, W Schempp, T F Wienker
Deutsche Medizinische Wochenschrift (1946)
|
October 29, 1976
[Color blindness: in high school students less often than in elementary school pupils]
K Feig, T F Wienker, H H Ropers
Human Genetics
|
June 29, 1976
Fabry's disease: heterozygote detection by hair root analysis
T Grimm, T F Wienker, H H Ropers
Human Genetics
|
February 1, 1980
The presence of androgen-binding receptors in genital and nongenital skin fibroblasts
J Herfert, T F Wienker, H H Ropers
Nucleic Acids Research
|
April 25, 1989
A BAM HI RFLP at the human tyrosine aminotransferase (TAT) gene locus at 16q
B Wullich, E Natt, T F Wienker, et al.
Page
of 11