Search research articles
Contact Us
Filters
Showing results (21-30 of 87) with videos related to
Page
of 9
Sort By:
British Journal of Haematology
|
March 23, 1999
Identification of the inverted chromosome 16 using chromosome painting
P N Rao, W L Flejter, S Rahi, et al.
Genomics
|
June 1, 1996
Localization and physical mapping of genes encoding the A+U-rich element RNA-binding protein AUF1 to human chromosomes 4 and X
B J Wagner, L Long, P N Rao, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1988
Translocation (8;16)(p11;p13) in patients with acute monocytic leukemias. An evolving syndrome?
B L Powell, J W McNay, S Brown, et al.
American Journal of Medical Genetics
|
April 1, 1989
Nonketotic hyperglycinemia in a patient with the 9p- syndrome
B K Burton, M J Pettenati, S M Block, et al.
American Journal of Medical Genetics
|
May 1, 1991
Partial deletion of chromosome 6p: delineation of the syndrome
C G Palmer, P Bader, M L Slovak, et al.
Human Genetics
|
August 1, 1994
Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome
P N Rao, K Klinepeter, W Stewart, et al.
Clinical Genetics
|
September 17, 2003
Ring chromosome 17: phenotype variation by deletion size
V Shashi, J R White, M J Pettenati, et al.
Cancer Genetics and Cytogenetics
|
July 15, 1994
Trisomy 5 as the sole abnormality in acute lymphoblastic leukemia. A second case and review
P N Rao, D Buss, S Brown, et al.
Human Genetics
|
January 1, 1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome
A P Amarose, P R Huttenlocher, R M Sprudzs, et al.
Annals of Hematology
|
January 25, 2002
Primary malignant lymphoma of uterine corpus: case report and review of the literature
S I Renno, W S Moreland, M J Pettenati, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 87) with videos related to
Sort By:
Page
of 9
British Journal of Haematology
|
March 23, 1999
Identification of the inverted chromosome 16 using chromosome painting
P N Rao, W L Flejter, S Rahi, et al.
Genomics
|
June 1, 1996
Localization and physical mapping of genes encoding the A+U-rich element RNA-binding protein AUF1 to human chromosomes 4 and X
B J Wagner, L Long, P N Rao, et al.
Cancer Genetics and Cytogenetics
|
November 1, 1988
Translocation (8;16)(p11;p13) in patients with acute monocytic leukemias. An evolving syndrome?
B L Powell, J W McNay, S Brown, et al.
American Journal of Medical Genetics
|
April 1, 1989
Nonketotic hyperglycinemia in a patient with the 9p- syndrome
B K Burton, M J Pettenati, S M Block, et al.
American Journal of Medical Genetics
|
May 1, 1991
Partial deletion of chromosome 6p: delineation of the syndrome
C G Palmer, P Bader, M L Slovak, et al.
Human Genetics
|
August 1, 1994
Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome
P N Rao, K Klinepeter, W Stewart, et al.
Clinical Genetics
|
September 17, 2003
Ring chromosome 17: phenotype variation by deletion size
V Shashi, J R White, M J Pettenati, et al.
Cancer Genetics and Cytogenetics
|
July 15, 1994
Trisomy 5 as the sole abnormality in acute lymphoblastic leukemia. A second case and review
P N Rao, D Buss, S Brown, et al.
Human Genetics
|
January 1, 1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome
A P Amarose, P R Huttenlocher, R M Sprudzs, et al.
Annals of Hematology
|
January 25, 2002
Primary malignant lymphoma of uterine corpus: case report and review of the literature
S I Renno, W S Moreland, M J Pettenati, et al.
Page
of 9