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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 Medical Genetics
|
October 16, 1996
A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13
M G Butler, S L Christian, T Kubota, et al.
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.
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.
Genomics
|
June 1, 1990
Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3
S A Ledbetter, M R Wallace, F S Collins, et al.
Nucleic Acids Research
|
November 11, 1987
An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]
S Kondoleon, P van Tuinen, D H Ledbetter, et al.
Molecular and Cellular Biology
|
June 1, 1983
Deletion and amplification of the HGPRT locus in Chinese hamster cells
J C Fuscoe, R G Fenwick, D H Ledbetter, et al.
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of 26
Search research articles
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Showing results (51-60 of 251) with videos related to
Sort By:
Page
of 26
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 Medical Genetics
|
October 16, 1996
A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13
M G Butler, S L Christian, T Kubota, et al.
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.
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.
Genomics
|
June 1, 1990
Human chromosome 17 NotI linking clones and their use in long-range restriction mapping of the Miller-Dieker chromosome region (MDCR) in 17p13.3
S A Ledbetter, M R Wallace, F S Collins, et al.
Nucleic Acids Research
|
November 11, 1987
An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 No. D17S21]
S Kondoleon, P van Tuinen, D H Ledbetter, et al.
Molecular and Cellular Biology
|
June 1, 1983
Deletion and amplification of the HGPRT locus in Chinese hamster cells
J C Fuscoe, R G Fenwick, D H Ledbetter, et al.
Page
of 26