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The Journal of Urology
|
December 11, 1992
The transmission of vesicoureteral reflux from parent to child
H N Noe, R J Wyatt, J N Peeden, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1
R E Magenis, T Donlon, M Parks, et al.
Journal of Clinical & Laboratory Immunology
|
December 1, 1989
C4 and Bf phenotypes in black and Caucasian patients with childhood onset insulin dependent diabetes mellitus
C Wang, M L Rivas, G A Burghen, et al.
American Journal of Medical Genetics
|
May 1, 1990
Infantile hypophosphatasia: autosomal recessive transmission to two related sibships
C A Moore, J C Ward, M L Rivas, et al.
The Journal of Pediatrics
|
May 1, 1990
Regional variation in C4 phenotype in patients with IgA nephropathy
R J Wyatt, M L Rivas, F P Schena, et al.
American Journal of Medical Genetics
|
March 1, 1992
Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes
S A Tharapel, R S Wilroy, A M Keath, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Linkage study of antithrombin III
E W Lovrien, R E Magenis, M L Rivas, et al.
Clinical Genetics
|
May 20, 1999
Interpupillary distance in a normal black population
E K Pivnick, M L Rivas, E A Tolley, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16
E W Lovrien, R E Magenis, M L Rivas, et al.
American Journal of Human Genetics
|
May 1, 1972
Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci
P S Harper, M L Rivas, W B Bias, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
The Journal of Urology
|
December 11, 1992
The transmission of vesicoureteral reflux from parent to child
H N Noe, R J Wyatt, J N Peeden, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1
R E Magenis, T Donlon, M Parks, et al.
Journal of Clinical & Laboratory Immunology
|
December 1, 1989
C4 and Bf phenotypes in black and Caucasian patients with childhood onset insulin dependent diabetes mellitus
C Wang, M L Rivas, G A Burghen, et al.
American Journal of Medical Genetics
|
May 1, 1990
Infantile hypophosphatasia: autosomal recessive transmission to two related sibships
C A Moore, J C Ward, M L Rivas, et al.
The Journal of Pediatrics
|
May 1, 1990
Regional variation in C4 phenotype in patients with IgA nephropathy
R J Wyatt, M L Rivas, F P Schena, et al.
American Journal of Medical Genetics
|
March 1, 1992
Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes
S A Tharapel, R S Wilroy, A M Keath, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Linkage study of antithrombin III
E W Lovrien, R E Magenis, M L Rivas, et al.
Clinical Genetics
|
May 20, 1999
Interpupillary distance in a normal black population
E K Pivnick, M L Rivas, E A Tolley, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16
E W Lovrien, R E Magenis, M L Rivas, et al.
American Journal of Human Genetics
|
May 1, 1972
Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci
P S Harper, M L Rivas, W B Bias, et al.
Page
of 4