Search research articles
Contact Us
Filters
Showing results (181-190 of 411) with videos related to
Page
of 42
Sort By:
Human Heredity
|
January 1, 1979
Pericentric inversions of chromosome number 9: benign or harmful?
P N Howard-Peebles, G R Stoddard
Enzyme
|
January 1, 1976
Effects of heparin on lipolytic enzyme activities in vivo and in vitro
J Patelski, Z Waligora, A N Howard
American Journal of Mental Deficiency
|
November 1, 1979
A tera-X female: cytogenetic testing, dermatoglyphic studies, and speech impairment
P N Howard-Peebles, R I Markiton
European Journal of Nuclear Medicine
|
January 1, 1985
Thyroid dysgenesis in monozygotic twins: variants identified by scintigraphy
R McLean, N Howard, I P Murray
Cytogenetics and Cell Genetics
|
January 1, 1979
Mental retardation, marker X chromosomes, and silver-staining (NORs)
P N Howard-Peebles, W M Howell
American Journal of Medical Genetics
|
January 1, 1984
Recombination between the fragile X and G6PD
P N Howard-Peebles, A J Carroll
Human Heredity
|
January 1, 1980
Duplication of region 2q31 leads to 2qter in a family with 2/9 translocation
P N Howard-Peebles, J P Goldsmith
Human Genetics
|
September 1, 1979
X-linked mental retardation with macro-orchidism and marker X chromosomes
P N Howard-Peebles, G R Stoddard
American Journal of Medical Genetics
|
January 1, 1984
X-linked mental retardation revisited
P N Howard-Peebles, S F Roberts
American Journal of Medical Genetics
|
September 1, 1983
On the nature of folic-acid-sensitive fragile sites in human chromosomes: an hypothesis
C L Krumdieck, P N Howard-Peebles
Page
of 42
Search research articles
Search
Showing results (181-190 of 411) with videos related to
Sort By:
Page
of 42
Human Heredity
|
January 1, 1979
Pericentric inversions of chromosome number 9: benign or harmful?
P N Howard-Peebles, G R Stoddard
Enzyme
|
January 1, 1976
Effects of heparin on lipolytic enzyme activities in vivo and in vitro
J Patelski, Z Waligora, A N Howard
American Journal of Mental Deficiency
|
November 1, 1979
A tera-X female: cytogenetic testing, dermatoglyphic studies, and speech impairment
P N Howard-Peebles, R I Markiton
European Journal of Nuclear Medicine
|
January 1, 1985
Thyroid dysgenesis in monozygotic twins: variants identified by scintigraphy
R McLean, N Howard, I P Murray
Cytogenetics and Cell Genetics
|
January 1, 1979
Mental retardation, marker X chromosomes, and silver-staining (NORs)
P N Howard-Peebles, W M Howell
American Journal of Medical Genetics
|
January 1, 1984
Recombination between the fragile X and G6PD
P N Howard-Peebles, A J Carroll
Human Heredity
|
January 1, 1980
Duplication of region 2q31 leads to 2qter in a family with 2/9 translocation
P N Howard-Peebles, J P Goldsmith
Human Genetics
|
September 1, 1979
X-linked mental retardation with macro-orchidism and marker X chromosomes
P N Howard-Peebles, G R Stoddard
American Journal of Medical Genetics
|
January 1, 1984
X-linked mental retardation revisited
P N Howard-Peebles, S F Roberts
American Journal of Medical Genetics
|
September 1, 1983
On the nature of folic-acid-sensitive fragile sites in human chromosomes: an hypothesis
C L Krumdieck, P N Howard-Peebles
Page
of 42