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R L Nussbaum

Showing results (21-30 of 115) with videos related to

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Genomics|July 8, 1998
Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic miceC Lavedan, E Grabczyk, K Usdin, et al.
American Journal of Medical Genetics|January 1, 1986
Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting maleD H Ledbetter, S D Airhart, R L Nussbaum
American Journal of Medical Genetics|January 1, 1986
Caffeine enhances fragile (X) expression in somatic cell hybridsD H Ledbetter, S D Airhart, R L Nussbaum
Nature|November 13, 1986
Implications of fragile X expression in normal males for the nature of the mutationD H Ledbetter, S A Ledbetter, R L Nussbaum
The Journal of Clinical Investigation|January 1, 1987
Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphismsD N Silver, R A Lewis, R L Nussbaum
The Journal of Clinical Investigation|May 1, 1987
Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivationJ M Puck, R L Nussbaum, M E Conley
American Journal of Medical Genetics|January 1, 1986
Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesisR L Nussbaum, S D Airhart, D H Ledbetter
Nucleic Acids Research|July 11, 1989
Detection of translocation breakpoints by pulsed field gel analysis: practical considerationsD S Reilly, D M Sosnoski, R L Nussbaum
American Journal of Medical Genetics|January 1, 1986
A rodent-human hybrid containing Xq24-qter translocated to a hamster chromosome expresses the Xq27 folate-sensitive fragile siteR L Nussbaum, S D Airhart, D H Ledbetter
Genomics|September 1, 1990
Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndromeD S Reilly, R A Lewis, R L Nussbaum
Pageof 12

Showing results (21-30 of 115) with videos related to

Sort By:
Pageof 12
Genomics|July 8, 1998
Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic miceC Lavedan, E Grabczyk, K Usdin, et al.
American Journal of Medical Genetics|January 1, 1986
Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting maleD H Ledbetter, S D Airhart, R L Nussbaum
American Journal of Medical Genetics|January 1, 1986
Caffeine enhances fragile (X) expression in somatic cell hybridsD H Ledbetter, S D Airhart, R L Nussbaum
Nature|November 13, 1986
Implications of fragile X expression in normal males for the nature of the mutationD H Ledbetter, S A Ledbetter, R L Nussbaum
The Journal of Clinical Investigation|January 1, 1987
Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphismsD N Silver, R A Lewis, R L Nussbaum
The Journal of Clinical Investigation|May 1, 1987
Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivationJ M Puck, R L Nussbaum, M E Conley
American Journal of Medical Genetics|January 1, 1986
Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesisR L Nussbaum, S D Airhart, D H Ledbetter
Nucleic Acids Research|July 11, 1989
Detection of translocation breakpoints by pulsed field gel analysis: practical considerationsD S Reilly, D M Sosnoski, R L Nussbaum
American Journal of Medical Genetics|January 1, 1986
A rodent-human hybrid containing Xq24-qter translocated to a hamster chromosome expresses the Xq27 folate-sensitive fragile siteR L Nussbaum, S D Airhart, D H Ledbetter
Genomics|September 1, 1990
Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndromeD S Reilly, R A Lewis, R L Nussbaum
Pageof 12