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S L Nolin

Showing results (11-20 of 21) with videos related to

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American Journal of Medical Genetics|April 20, 1999
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detectionC Dobkin, X Ding, S Li, et al.
Journal of Genetic Counseling|November 16, 2013
Molecular carrier testing for the fragile X syndrome: Issues for genetic counselorsJ L Berliner, F N Shapiro, S L Nolin, et al.
American Journal of Human Genetics|August 27, 1998
Examination of factors associated with instability of the FMR1 CGG repeatA E Ashley-Koch, H Robinson, A E Glicksman, et al.
American Journal of Medical Genetics|April 1, 1992
New York State screening program for fragile X syndrome: a progress reportS L Nolin, D A Snider, E C Jenkins, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue differences in fragile X mosaics: mosaicism in blood cells may differ greatly from skinC S Dobkin, S L Nolin, I Cohen, et al.
Human Genetics|January 1, 1984
Distal duplication 14q: report of three cases and further delineation of the syndromeS L Sklower, E C Jenkins, S L Nolin, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X screening program in New York StateS L Nolin, D A Snider, E C Jenkins, et al.
American Journal of Human Genetics|December 1, 1996
Familial transmission of the FMR1 CGG repeatS L Nolin, F A Lewis, L L Ye, et al.
American Journal of Medical Genetics|April 20, 1999
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodiesE C Jenkins, G Y Wen, K S Kim, et al.
American Journal of Human Genetics|March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 20, 1999
Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detectionC Dobkin, X Ding, S Li, et al.
Journal of Genetic Counseling|November 16, 2013
Molecular carrier testing for the fragile X syndrome: Issues for genetic counselorsJ L Berliner, F N Shapiro, S L Nolin, et al.
American Journal of Human Genetics|August 27, 1998
Examination of factors associated with instability of the FMR1 CGG repeatA E Ashley-Koch, H Robinson, A E Glicksman, et al.
American Journal of Medical Genetics|April 1, 1992
New York State screening program for fragile X syndrome: a progress reportS L Nolin, D A Snider, E C Jenkins, et al.
American Journal of Medical Genetics|August 9, 1996
Tissue differences in fragile X mosaics: mosaicism in blood cells may differ greatly from skinC S Dobkin, S L Nolin, I Cohen, et al.
Human Genetics|January 1, 1984
Distal duplication 14q: report of three cases and further delineation of the syndromeS L Sklower, E C Jenkins, S L Nolin, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X screening program in New York StateS L Nolin, D A Snider, E C Jenkins, et al.
American Journal of Human Genetics|December 1, 1996
Familial transmission of the FMR1 CGG repeatS L Nolin, F A Lewis, L L Ye, et al.
American Journal of Medical Genetics|April 20, 1999
Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodiesE C Jenkins, G Y Wen, K S Kim, et al.
American Journal of Human Genetics|March 21, 2000
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American populationD C Crawford, C E Schwartz, K L Meadows, et al.
Pageof 3