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American Journal of Medical Genetics
|
April 1, 1992
Fra(X) prenatal diagnosis: are endoreduplicated and polyploid cells useful diagnostic criteria?
M S Krawczun, C J Duncan, S L Stark-Houck, et al.
Progress in Clinical and Biological Research
|
January 1, 1991
Molecular markers of fragile X: application to males at risk in fragile X families
W T Brown, P Goonewardena, A C Gross, et al.
American Journal of Medical Genetics
|
April 1, 1992
Dialyzed fetal bovine serum increases cytogenetic fragile X expression
E C Jenkins, C J Duncan, H Gu, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Clinical features of a neuropathologically verified familial Alzheimer's cohort with onset in the fourth decade: comparison with senile onset Alzheimer's disease and etiopathogenic implications
B Reisberg, S H Ferris, E Franssen, et al.
Journal of Medical Genetics
|
October 1, 1980
A liveborn case of 49,XXXY, + 18
N B Kardon, A L Berger, M Elice, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1985
A comparison of adult and childhood progerias: Werner syndrome and Hutchinson-Gilford progeria syndrome
W T Brown, F J Kieras, G E Houck, et al.
American Journal of Medical Genetics
|
May 20, 1999
Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease
N Zhong, W Ju, W T Brown, et al.
American Journal of Medical Genetics
|
February 1, 1991
Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males
I L Cohen, P M Vietze, V Sudhalter, et al.
Journal of Neurogenetics
|
June 1, 1987
Assignment of proteins to human chromosome 21 using two-dimensional gel electrophoresis and somatic cell genetics: an approach to the study of Down syndrome
E A Devine-Gage, W T Brown, E C Jenkins, et al.
American Journal of Human Genetics
|
January 1, 1984
Verbal vs. nonverbal ability, fragile X syndrome, and heterozygous carriers
C M Miezejeski, E C Jenkins, A L Hill, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 146) with videos related to
Sort By:
Page
of 15
American Journal of Medical Genetics
|
April 1, 1992
Fra(X) prenatal diagnosis: are endoreduplicated and polyploid cells useful diagnostic criteria?
M S Krawczun, C J Duncan, S L Stark-Houck, et al.
Progress in Clinical and Biological Research
|
January 1, 1991
Molecular markers of fragile X: application to males at risk in fragile X families
W T Brown, P Goonewardena, A C Gross, et al.
American Journal of Medical Genetics
|
April 1, 1992
Dialyzed fetal bovine serum increases cytogenetic fragile X expression
E C Jenkins, C J Duncan, H Gu, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Clinical features of a neuropathologically verified familial Alzheimer's cohort with onset in the fourth decade: comparison with senile onset Alzheimer's disease and etiopathogenic implications
B Reisberg, S H Ferris, E Franssen, et al.
Journal of Medical Genetics
|
October 1, 1980
A liveborn case of 49,XXXY, + 18
N B Kardon, A L Berger, M Elice, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1985
A comparison of adult and childhood progerias: Werner syndrome and Hutchinson-Gilford progeria syndrome
W T Brown, F J Kieras, G E Houck, et al.
American Journal of Medical Genetics
|
May 20, 1999
Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease
N Zhong, W Ju, W T Brown, et al.
American Journal of Medical Genetics
|
February 1, 1991
Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males
I L Cohen, P M Vietze, V Sudhalter, et al.
Journal of Neurogenetics
|
June 1, 1987
Assignment of proteins to human chromosome 21 using two-dimensional gel electrophoresis and somatic cell genetics: an approach to the study of Down syndrome
E A Devine-Gage, W T Brown, E C Jenkins, et al.
American Journal of Human Genetics
|
January 1, 1984
Verbal vs. nonverbal ability, fragile X syndrome, and heterozygous carriers
C M Miezejeski, E C Jenkins, A L Hill, et al.
Page
of 15