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W P Robinson

Showing results (61-70 of 115) with videos related to

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Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Genomics|May 15, 1996
Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletionW P Robinson, J Waslynka, F Bernasconi, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Clinical and molecular analysis of five inv dup(15) patientsW P Robinson, F Binkert, R Giné, et al.
American Journal of Human Genetics|January 1, 1994
Maternal uniparental disomy 22 has no impact on the phenotypeA A Schinzel, S Basaran, F Bernasconi, et al.
American Journal of Human Genetics|December 18, 1997
Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicismA W Lau, C J Brown, M Peñaherrera, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
Placenta|October 16, 2010
Evaluating DNA methylation and gene expression variability in the human term placentaL Avila, R K Yuen, D Diego-Alvarez, et al.
American Journal of Human Genetics|February 1, 1995
Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selectionW P Robinson, F Binkert, F Bernasconi, et al.
Prenatal Diagnosis|March 26, 2005
Prenatally detected trisomy 20 mosaicismW P Robinson, B McGillivray, M E S Lewis, et al.
American Journal of Medical Genetics|March 17, 2001
Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13)E Rajcan-Separovic, W P Robinson, M Stephenson, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Genomics|May 15, 1996
Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletionW P Robinson, J Waslynka, F Bernasconi, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Clinical and molecular analysis of five inv dup(15) patientsW P Robinson, F Binkert, R Giné, et al.
American Journal of Human Genetics|January 1, 1994
Maternal uniparental disomy 22 has no impact on the phenotypeA A Schinzel, S Basaran, F Bernasconi, et al.
American Journal of Human Genetics|December 18, 1997
Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicismA W Lau, C J Brown, M Peñaherrera, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
Placenta|October 16, 2010
Evaluating DNA methylation and gene expression variability in the human term placentaL Avila, R K Yuen, D Diego-Alvarez, et al.
American Journal of Human Genetics|February 1, 1995
Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selectionW P Robinson, F Binkert, F Bernasconi, et al.
Prenatal Diagnosis|March 26, 2005
Prenatally detected trisomy 20 mosaicismW P Robinson, B McGillivray, M E S Lewis, et al.
American Journal of Medical Genetics|March 17, 2001
Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13)E Rajcan-Separovic, W P Robinson, M Stephenson, et al.
Pageof 12