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American Journal of Medical Genetics
|
August 9, 1996
Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population
K L Meadows, D Pettay, J Newman, et al.
American Journal of Human Genetics
|
September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies
C E Aston, S L Sherman, N E Morton, et al.
American Journal of Human Genetics
|
June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency
S L Sherman, C E Aston, N E Morton, et al.
Genetic Epidemiology
|
January 1, 1997
Sequential sib-pair and association studies to detect genes in quantitative traits
A Savage, F Sun, D C Crawford, et al.
Human Reproduction (Oxford, England)
|
March 4, 2008
Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study
J Rohr, E G Allen, K Charen, et al.
Human Genetics
|
September 27, 2015
Association between telomere length and chromosome 21 nondisjunction in the oocyte
I Albizua, B L Rambo-Martin, E G Allen, et al.
Genes, Chromosomes & Cancer
|
February 1, 1994
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome
G J Riggins, S L Sherman, C N Phillips, et al.
Annals of Neurology
|
June 1, 1992
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis
S G Ryan, S L Sherman, J C Terry, et al.
Progress in Clinical and Biological Research
|
January 1, 1991
Laboratory aspects of prenatal fra(X) detection
E C Jenkins, M S Krawczun, S E Brooks, et al.
Hospitals
|
August 16, 1985
Health promotion programs flourishing: survey
C K Ross, S L Sherman, K L Berg, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 109) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics
|
August 9, 1996
Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population
K L Meadows, D Pettay, J Newman, et al.
American Journal of Human Genetics
|
September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies
C E Aston, S L Sherman, N E Morton, et al.
American Journal of Human Genetics
|
June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency
S L Sherman, C E Aston, N E Morton, et al.
Genetic Epidemiology
|
January 1, 1997
Sequential sib-pair and association studies to detect genes in quantitative traits
A Savage, F Sun, D C Crawford, et al.
Human Reproduction (Oxford, England)
|
March 4, 2008
Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study
J Rohr, E G Allen, K Charen, et al.
Human Genetics
|
September 27, 2015
Association between telomere length and chromosome 21 nondisjunction in the oocyte
I Albizua, B L Rambo-Martin, E G Allen, et al.
Genes, Chromosomes & Cancer
|
February 1, 1994
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome
G J Riggins, S L Sherman, C N Phillips, et al.
Annals of Neurology
|
June 1, 1992
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis
S G Ryan, S L Sherman, J C Terry, et al.
Progress in Clinical and Biological Research
|
January 1, 1991
Laboratory aspects of prenatal fra(X) detection
E C Jenkins, M S Krawczun, S E Brooks, et al.
Hospitals
|
August 16, 1985
Health promotion programs flourishing: survey
C K Ross, S L Sherman, K L Berg, et al.
Page
of 11