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W P Robinson

Showing results (31-40 of 115) with videos related to

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Frontiers in Genetics|September 22, 2023
eoPred: predicting the placental phenotype of early-onset preeclampsia using public DNA methylation dataI Fernández-Boyano, A M Inkster, V Yuan, et al.
Seminars in Reproductive Medicine|August 2, 2001
Skewed X inactivation and recurrent spontaneous abortionW P Robinson, C Beever, C J Brown, et al.
Human Genetics|January 1, 1992
Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin?A Schinzel, W P Robinson, A Bottani, et al.
Transactions - American Society for Artificial Internal Organs|January 1, 1978
Delineation of pump-induced thrombocytopenic responsesW P Robinson, L F Mockros, L Zuckerman, et al.
Clinical Pharmacology and Therapeutics|October 11, 2012
Prenatal and perinatal environmental influences on the human fetal and placental epigenomeK Hogg, E M Price, C W Hanna, et al.
Placenta|January 28, 2014
Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsiaJ D Blair, S Langlois, D E McFadden, et al.
Journal of Medical Genetics|May 1, 1994
Multiple origins of X chromosome tetrasomyW P Robinson, F Binkert, A A Schinzel, et al.
American Journal of Medical Genetics|May 9, 2001
Grandmaternal origin of an isochromosome 18p present in two maternal half-sistersJ Boyle, K Sangha, F Dill, et al.
Genetics|November 1, 1991
Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA dataW P Robinson, A Cambon-Thomsen, N Borot, et al.
American Journal of Medical Genetics|August 22, 1997
Novel case of del(17)(q23.1q23.3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24)E C Mickelson, W P Robinson, M A Hrynchak, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Frontiers in Genetics|September 22, 2023
eoPred: predicting the placental phenotype of early-onset preeclampsia using public DNA methylation dataI Fernández-Boyano, A M Inkster, V Yuan, et al.
Seminars in Reproductive Medicine|August 2, 2001
Skewed X inactivation and recurrent spontaneous abortionW P Robinson, C Beever, C J Brown, et al.
Human Genetics|January 1, 1992
Prader-Willi or Angelman syndrome in familial 15q11----q13 deletion of maternal origin?A Schinzel, W P Robinson, A Bottani, et al.
Transactions - American Society for Artificial Internal Organs|January 1, 1978
Delineation of pump-induced thrombocytopenic responsesW P Robinson, L F Mockros, L Zuckerman, et al.
Clinical Pharmacology and Therapeutics|October 11, 2012
Prenatal and perinatal environmental influences on the human fetal and placental epigenomeK Hogg, E M Price, C W Hanna, et al.
Placenta|January 28, 2014
Overlapping DNA methylation profile between placentas with trisomy 16 and early-onset preeclampsiaJ D Blair, S Langlois, D E McFadden, et al.
Journal of Medical Genetics|May 1, 1994
Multiple origins of X chromosome tetrasomyW P Robinson, F Binkert, A A Schinzel, et al.
American Journal of Medical Genetics|May 9, 2001
Grandmaternal origin of an isochromosome 18p present in two maternal half-sistersJ Boyle, K Sangha, F Dill, et al.
Genetics|November 1, 1991
Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA dataW P Robinson, A Cambon-Thomsen, N Borot, et al.
American Journal of Medical Genetics|August 22, 1997
Novel case of del(17)(q23.1q23.3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24)E C Mickelson, W P Robinson, M A Hrynchak, et al.
Pageof 12