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American Journal of Medical Genetics
|
September 1, 1993
Genetic syndromes and uniparental disomy: a study of 16 cases of Brachmann-de Lange syndrome
L G Shaffer, J Overhauser, L G Jackson, et al.
American Journal of Medical Genetics
|
March 1, 1993
Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation
L G Shaffer, J T Hecht, D H Ledbetter, et al.
Human Genetics
|
August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13
A L Pettigrew, F Greenberg, C T Caskey, et al.
American Journal of Human Genetics
|
March 1, 1990
Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndrome
D J Kwiatkowski, L Aklog, D H Ledbetter, et al.
Trends in Neurosciences
|
August 17, 2001
LIS1: from cortical malformation to essential protein of cellular dynamics
R J Leventer, C Cardoso, D H Ledbetter, et al.
Genome Research
|
August 1, 1996
14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome region
S S Chong, A Tanigami, A V Roschke, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1990
Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines
P Lichter, S A Ledbetter, D H Ledbetter, et al.
American Journal of Medical Genetics
|
March 1, 1994
Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions
S Saitoh, A Mutirangura, A Kuwano, et al.
American Journal of Obstetrics and Gynecology
|
November 1, 1989
Integration of the transabdominal technique into an ongoing chorionic villus sampling program
K L Copeland, R J Carpenter, K R Fenolio, et al.
Human Genetics
|
August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center
A L Pettigrew, E R McCabe, F F Elder, et al.
Page
of 39
Search research articles
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Showing results (71-80 of 388) with videos related to
Sort By:
Page
of 39
American Journal of Medical Genetics
|
September 1, 1993
Genetic syndromes and uniparental disomy: a study of 16 cases of Brachmann-de Lange syndrome
L G Shaffer, J Overhauser, L G Jackson, et al.
American Journal of Medical Genetics
|
March 1, 1993
Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation
L G Shaffer, J T Hecht, D H Ledbetter, et al.
Human Genetics
|
August 1, 1991
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13
A L Pettigrew, F Greenberg, C T Caskey, et al.
American Journal of Human Genetics
|
March 1, 1990
Identification of the functional profilin gene, its localization to chromosome subband 17p13.3, and demonstration of its deletion in some patients with Miller-Dieker syndrome
D J Kwiatkowski, L Aklog, D H Ledbetter, et al.
Trends in Neurosciences
|
August 17, 2001
LIS1: from cortical malformation to essential protein of cellular dynamics
R J Leventer, C Cardoso, D H Ledbetter, et al.
Genome Research
|
August 1, 1996
14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome region
S S Chong, A Tanigami, A V Roschke, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1990
Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines
P Lichter, S A Ledbetter, D H Ledbetter, et al.
American Journal of Medical Genetics
|
March 1, 1994
Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions
S Saitoh, A Mutirangura, A Kuwano, et al.
American Journal of Obstetrics and Gynecology
|
November 1, 1989
Integration of the transabdominal technique into an ongoing chorionic villus sampling program
K L Copeland, R J Carpenter, K R Fenolio, et al.
Human Genetics
|
August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation center
A L Pettigrew, E R McCabe, F F Elder, et al.
Page
of 39