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Cytogenetics and Cell Genetics
|
January 1, 1991
Second international workshop on human chromosome 17
P R Fain, E Solomon, D H Ledbetter
American Journal of Medical Genetics
|
December 1, 1987
Neonatal diagnosis of Prader-Willi syndrome and its implications
F Greenberg, F F Elder, D H Ledbetter
Human Genetics
|
April 1, 1991
Determination of the origin of nondisjunction in a 49,XXXXY male using hypervariable dinucleotide repeat sequences
T H Huang, F Greenberg, D H Ledbetter
Clinical Genetics
|
November 1, 1983
Cystic hygroma and hydrops fetalis in a fetus with trisomy 13
F Greenberg, R J Carpenter, D H Ledbetter
Genomics
|
March 3, 1999
Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS)
N Matsumoto, D T Pilz, D H Ledbetter
American Journal of Medical Genetics
|
January 1, 1986
Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male
D H Ledbetter, S D Airhart, R L Nussbaum
American Journal of Medical Genetics
|
January 1, 1986
Caffeine enhances fragile (X) expression in somatic cell hybrids
D H Ledbetter, S D Airhart, R L Nussbaum
Cytogenetic and Genome Research
|
November 17, 2004
The dynamic nature and evolutionary history of subtelomeric and pericentromeric regions
S K Mewborn, C Lese Martin, D H Ledbetter
Genetic Testing
|
August 28, 1999
A simple VNTR-PCR method for detecting maternal cell contamination in prenatal diagnosis
J R Batanian, D H Ledbetter, R G Fenwick
Nature
|
November 13, 1986
Implications of fragile X expression in normal males for the nature of the mutation
D H Ledbetter, S A Ledbetter, R L Nussbaum
Page
of 26
Search research articles
Search
Showing results (21-30 of 251) with videos related to
Sort By:
Page
of 26
Cytogenetics and Cell Genetics
|
January 1, 1991
Second international workshop on human chromosome 17
P R Fain, E Solomon, D H Ledbetter
American Journal of Medical Genetics
|
December 1, 1987
Neonatal diagnosis of Prader-Willi syndrome and its implications
F Greenberg, F F Elder, D H Ledbetter
Human Genetics
|
April 1, 1991
Determination of the origin of nondisjunction in a 49,XXXXY male using hypervariable dinucleotide repeat sequences
T H Huang, F Greenberg, D H Ledbetter
Clinical Genetics
|
November 1, 1983
Cystic hygroma and hydrops fetalis in a fetus with trisomy 13
F Greenberg, R J Carpenter, D H Ledbetter
Genomics
|
March 3, 1999
Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS)
N Matsumoto, D T Pilz, D H Ledbetter
American Journal of Medical Genetics
|
January 1, 1986
Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male
D H Ledbetter, S D Airhart, R L Nussbaum
American Journal of Medical Genetics
|
January 1, 1986
Caffeine enhances fragile (X) expression in somatic cell hybrids
D H Ledbetter, S D Airhart, R L Nussbaum
Cytogenetic and Genome Research
|
November 17, 2004
The dynamic nature and evolutionary history of subtelomeric and pericentromeric regions
S K Mewborn, C Lese Martin, D H Ledbetter
Genetic Testing
|
August 28, 1999
A simple VNTR-PCR method for detecting maternal cell contamination in prenatal diagnosis
J R Batanian, D H Ledbetter, R G Fenwick
Nature
|
November 13, 1986
Implications of fragile X expression in normal males for the nature of the mutation
D H Ledbetter, S A Ledbetter, R L Nussbaum
Page
of 26