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Nature
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March 25, 1976
Increased frequency of heterozygotes for alpha1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21
R M Fineman, K K Kidd, A M Johnson, et al.
The Journal of Cell Biology
|
September 1, 1984
Amplification of sodium- and potassium-activated adenosinetriphosphatase in HeLa cells by ouabain step selection
J F Ash, R M Fineman, T Kalka, et al.
American Journal of Medical Genetics
|
January 1, 1980
Holoprosencephaly in a Down syndrome child
S Y Pi, R M Fineman, S D Wing, et al.
Cancer Genetics and Cytogenetics
|
July 1, 1983
Sister chromatid exchange: variation by age, sex, smoking, and breast cancer status
G K Livingston, L A Cannon, D T Bishop, et al.
Pediatrics
|
November 1, 1975
Trisomy 8 mosaicism syndrome
R M Fineman, R C Ablow, R O Howard, et al.
American Journal of Ophthalmology
|
April 1, 1979
Unilateral cryptophthalmia
R O Howard, R M Fineman, B Anderson, et al.
Pediatrics
|
April 1, 1978
Chromosome 3 duplication q/deletion p syndrome
R M Fineman, F Hecht, R C Ablow, et al.
Cancer
|
August 15, 1981
Monoblastic transformation in chronic myelogenous leukemia: presentation with massive hepatic involvement
S M Ondreyco, C R Kjeldsberg, R M Fineman, et al.
Molecular and Cellular Biology
|
April 1, 1986
Stable gene amplification and overexpression of sodium- and potassium-activated ATPase in HeLa cells
P G Pauw, M D Johnson, P Moore, et al.
American Journal of Medical Genetics
|
August 1, 1982
Spinal dysraphia as an autosomal dominant defect in four families
R M Fineman, L B Jorde, R A Martin, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
Nature
|
March 25, 1976
Increased frequency of heterozygotes for alpha1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21
R M Fineman, K K Kidd, A M Johnson, et al.
The Journal of Cell Biology
|
September 1, 1984
Amplification of sodium- and potassium-activated adenosinetriphosphatase in HeLa cells by ouabain step selection
J F Ash, R M Fineman, T Kalka, et al.
American Journal of Medical Genetics
|
January 1, 1980
Holoprosencephaly in a Down syndrome child
S Y Pi, R M Fineman, S D Wing, et al.
Cancer Genetics and Cytogenetics
|
July 1, 1983
Sister chromatid exchange: variation by age, sex, smoking, and breast cancer status
G K Livingston, L A Cannon, D T Bishop, et al.
Pediatrics
|
November 1, 1975
Trisomy 8 mosaicism syndrome
R M Fineman, R C Ablow, R O Howard, et al.
American Journal of Ophthalmology
|
April 1, 1979
Unilateral cryptophthalmia
R O Howard, R M Fineman, B Anderson, et al.
Pediatrics
|
April 1, 1978
Chromosome 3 duplication q/deletion p syndrome
R M Fineman, F Hecht, R C Ablow, et al.
Cancer
|
August 15, 1981
Monoblastic transformation in chronic myelogenous leukemia: presentation with massive hepatic involvement
S M Ondreyco, C R Kjeldsberg, R M Fineman, et al.
Molecular and Cellular Biology
|
April 1, 1986
Stable gene amplification and overexpression of sodium- and potassium-activated ATPase in HeLa cells
P G Pauw, M D Johnson, P Moore, et al.
American Journal of Medical Genetics
|
August 1, 1982
Spinal dysraphia as an autosomal dominant defect in four families
R M Fineman, L B Jorde, R A Martin, et al.
Page
of 5