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Human Genetics
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August 1, 1988
Expression of fragile sites in childhood acute lymphoblastic leukemia patients and normal controls
P N Rao, N A Heerema, C G Palmer
American Journal of Human Genetics
|
July 1, 1977
Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus
C G Palmer, J C Christian, A D Merritt
American Journal of Human Genetics
|
April 1, 1996
A general statistical model for detecting complex-trait loci by using affected relative pairs in a genome search
S L Smalley, J A Woodward, C G Palmer
Mutation Research
|
May 1, 1982
Effect of temperature variation on sister-chromatid exchange and cell-cycle duration in cultured human lymphocytes
M R Abdel-Fadil, C G Palmer, N Heerema
Human Genetics
|
January 1, 1982
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function
E A Keitges, C G Palmer, D D Weaver
Human Genetics
|
February 29, 1976
Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20
C G Palmer, C Poland, T Reed, et al.
American Journal of Medical Genetics
|
March 1, 1986
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
M G Butler, F J Meaney, C G Palmer
Human Genetics
|
January 1, 1988
Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysis
P N Rao, N A Heerema, C G Palmer
Cancer Genetics and Cytogenetics
|
June 1, 1985
Karyotypic and clinical findings in a consecutive series of children with acute lymphocytic leukemia
N A Heerema, C G Palmer, R L Baehner
American Journal of Medical Genetics
|
March 27, 1995
Marker chromosome 21 identified by microdissection and FISH
Y Sun, J Rubinstein, S Soukup, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 86) with videos related to
Sort By:
Page
of 9
Human Genetics
|
August 1, 1988
Expression of fragile sites in childhood acute lymphoblastic leukemia patients and normal controls
P N Rao, N A Heerema, C G Palmer
American Journal of Human Genetics
|
July 1, 1977
Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus
C G Palmer, J C Christian, A D Merritt
American Journal of Human Genetics
|
April 1, 1996
A general statistical model for detecting complex-trait loci by using affected relative pairs in a genome search
S L Smalley, J A Woodward, C G Palmer
Mutation Research
|
May 1, 1982
Effect of temperature variation on sister-chromatid exchange and cell-cycle duration in cultured human lymphocytes
M R Abdel-Fadil, C G Palmer, N Heerema
Human Genetics
|
January 1, 1982
Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function
E A Keitges, C G Palmer, D D Weaver
Human Genetics
|
February 29, 1976
Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20
C G Palmer, C Poland, T Reed, et al.
American Journal of Medical Genetics
|
March 1, 1986
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome
M G Butler, F J Meaney, C G Palmer
Human Genetics
|
January 1, 1988
Fragile sites induced by FUdR, caffeine, and aphidicolin. Their frequency, distribution, and analysis
P N Rao, N A Heerema, C G Palmer
Cancer Genetics and Cytogenetics
|
June 1, 1985
Karyotypic and clinical findings in a consecutive series of children with acute lymphocytic leukemia
N A Heerema, C G Palmer, R L Baehner
American Journal of Medical Genetics
|
March 27, 1995
Marker chromosome 21 identified by microdissection and FISH
Y Sun, J Rubinstein, S Soukup, et al.
Page
of 9