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Prenatal Diagnosis
|
January 1, 1992
Placental mosaicism in a case of 46,XY,-22,+t(22;22)(p11;q11) or i(22q) diagnosed at amniocentesis
N B Spinner, Z Gibas, R Kline, et al.
American Journal of Medical Genetics
|
May 22, 1995
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13
N B Spinner, E Zackai, S D Cheng, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1987
Chronic myelomonocytic leukemia in a patient with a familial t(6;16)(q13;q22) translocation
N B Spinner, B S Emanuel, E C Vonderheid, et al.
American Journal of Medical Genetics
|
March 1, 1993
Duplication 9q34-->qter identified by chromosome painting
N B Spinner, J N Lucas, M Poggensee, et al.
American Journal of Human Genetics
|
October 1, 1994
Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients
S D Cheng, N B Spinner, E H Zackai, et al.
The Journal of Biological Chemistry
|
June 27, 1998
The gene encoding human nuclear protein tyrosine phosphatase, PRL-1. Cloning, chromosomal localization, and identification of an intron enhancer
Y Peng, A Genin, N B Spinner, et al.
American Journal of Human Genetics
|
November 1, 1995
Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12
E B Rand, N B Spinner, D A Piccoli, et al.
Human Genetics
|
October 1, 1995
Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?
J E Pellegrino, R E Schnur, R Kline, et al.
Pediatric Neurology
|
September 1, 1996
Infantile spasms associated with proximal duplication of chromosome 15q
P M Bingham, N B Spinner, L Sovinsky, et al.
Annual Review of Public Health
|
January 1, 1984
Genetic epidemiology
M C King, G M Lee, N B Spinner, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 63) with videos related to
Sort By:
Page
of 7
Prenatal Diagnosis
|
January 1, 1992
Placental mosaicism in a case of 46,XY,-22,+t(22;22)(p11;q11) or i(22q) diagnosed at amniocentesis
N B Spinner, Z Gibas, R Kline, et al.
American Journal of Medical Genetics
|
May 22, 1995
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13
N B Spinner, E Zackai, S D Cheng, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1987
Chronic myelomonocytic leukemia in a patient with a familial t(6;16)(q13;q22) translocation
N B Spinner, B S Emanuel, E C Vonderheid, et al.
American Journal of Medical Genetics
|
March 1, 1993
Duplication 9q34-->qter identified by chromosome painting
N B Spinner, J N Lucas, M Poggensee, et al.
American Journal of Human Genetics
|
October 1, 1994
Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients
S D Cheng, N B Spinner, E H Zackai, et al.
The Journal of Biological Chemistry
|
June 27, 1998
The gene encoding human nuclear protein tyrosine phosphatase, PRL-1. Cloning, chromosomal localization, and identification of an intron enhancer
Y Peng, A Genin, N B Spinner, et al.
American Journal of Human Genetics
|
November 1, 1995
Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12
E B Rand, N B Spinner, D A Piccoli, et al.
Human Genetics
|
October 1, 1995
Mosaic loss of 15q11q13 in a patient with hypomelanosis of Ito: is there a role for the P gene?
J E Pellegrino, R E Schnur, R Kline, et al.
Pediatric Neurology
|
September 1, 1996
Infantile spasms associated with proximal duplication of chromosome 15q
P M Bingham, N B Spinner, L Sovinsky, et al.
Annual Review of Public Health
|
January 1, 1984
Genetic epidemiology
M C King, G M Lee, N B Spinner, et al.
Page
of 7