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American Journal of Medical Genetics
|
June 1, 1982
Marker X syndrome in an oriental family with probable transmission by a normal male
F A Rhoads, A C Oglesby, M Mayer, et al.
Human Genetics
|
January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome
M Mayer, M A Abruzzo, P A Jacobs, et al.
Journal of Medical Genetics
|
February 1, 1992
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding
P A Jacobs, C Browne, N Gregson, et al.
Annals of Human Genetics
|
January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysis
S L Sherman, N E Morton, P A Jacobs, et al.
Birth Defects Original Article Series
|
January 1, 1990
The parental origin of the missing or additional chromosome in 45,X and 47,XXX females
T Hassold, K Arnovitz, P A Jacobs, et al.
Human Molecular Genetics
|
March 1, 1994
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation
J N Macpherson, H Bullman, S A Youings, et al.
American Journal of Medical Genetics
|
April 1, 1992
Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype
N R Dennis, G Curtis, J N Macpherson, et al.
Human Genetics
|
January 1, 1983
A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome
P A Jacobs, M Mayer, J Matsuura, et al.
American Journal of Medical Genetics
|
October 1, 1987
Chromosome anomalies as predictors of recurrence risk for spontaneous abortion
N E Morton, D Chiu, C Holland, et al.
Bulletin of Mathematical Biology
|
January 1, 1997
A mathematical model for intracellular effects of toxins on DNA adduction and repair
D P Gaver, P A Jacobs, R L Carpenter, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 136) with videos related to
Sort By:
Page
of 14
American Journal of Medical Genetics
|
June 1, 1982
Marker X syndrome in an oriental family with probable transmission by a normal male
F A Rhoads, A C Oglesby, M Mayer, et al.
Human Genetics
|
January 1, 1985
A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome
M Mayer, M A Abruzzo, P A Jacobs, et al.
Journal of Medical Genetics
|
February 1, 1992
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding
P A Jacobs, C Browne, N Gregson, et al.
Annals of Human Genetics
|
January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysis
S L Sherman, N E Morton, P A Jacobs, et al.
Birth Defects Original Article Series
|
January 1, 1990
The parental origin of the missing or additional chromosome in 45,X and 47,XXX females
T Hassold, K Arnovitz, P A Jacobs, et al.
Human Molecular Genetics
|
March 1, 1994
Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation
J N Macpherson, H Bullman, S A Youings, et al.
American Journal of Medical Genetics
|
April 1, 1992
Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment, and absence of the Martin-Bell phenotype
N R Dennis, G Curtis, J N Macpherson, et al.
Human Genetics
|
January 1, 1983
A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome
P A Jacobs, M Mayer, J Matsuura, et al.
American Journal of Medical Genetics
|
October 1, 1987
Chromosome anomalies as predictors of recurrence risk for spontaneous abortion
N E Morton, D Chiu, C Holland, et al.
Bulletin of Mathematical Biology
|
January 1, 1997
A mathematical model for intracellular effects of toxins on DNA adduction and repair
D P Gaver, P A Jacobs, R L Carpenter, et al.
Page
of 14