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W P Robinson

Showing results (51-60 of 115) with videos related to

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American Journal of Medical Genetics|September 12, 2000
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell lineH Bruyère, R Rupps, B D Kuchinka, et al.
Human Genetics|September 1, 1993
Exclusively paternal X chromosomes in a girl with short statureA A Schinzel, W P Robinson, F Binkert, et al.
Clinical Genetics|October 7, 2005
Recurrent trisomy 21: four cases in three generationsJ L Gair, L Arbour, R Rupps, et al.
Progress in Clinical and Biological Research|January 1, 1989
Disease associations and disequilibrium mappingW P Robinson, P Kramer, H Payami, et al.
Molecular Human Reproduction|March 22, 2013
Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriageI Manokhina, C W Hanna, M D Stephenson, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
X-chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) caseM S Peñaherrera, S Ma, B Ho Yuen, et al.
Human Reproduction (Oxford, England)|September 20, 2006
Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriageA F Hirschfeld, R Jiang, W P Robinson, et al.
Clinical Genetics|August 1, 1993
Parental origin of the supernumerary chromosome in trisomy 18X Ya-gang, W P Robinson, R Spiegel, et al.
Human Reproduction (Oxford, England)|October 31, 2003
Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case reportS Ma, S S Tang, B Ho Yuen, et al.
American Journal of Medical Genetics|September 24, 2002
Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnanciesP J Yong, S A Marion, I J Barrett, et al.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|September 12, 2000
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell lineH Bruyère, R Rupps, B D Kuchinka, et al.
Human Genetics|September 1, 1993
Exclusively paternal X chromosomes in a girl with short statureA A Schinzel, W P Robinson, F Binkert, et al.
Clinical Genetics|October 7, 2005
Recurrent trisomy 21: four cases in three generationsJ L Gair, L Arbour, R Rupps, et al.
Progress in Clinical and Biological Research|January 1, 1989
Disease associations and disequilibrium mappingW P Robinson, P Kramer, H Payami, et al.
Molecular Human Reproduction|March 22, 2013
Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriageI Manokhina, C W Hanna, M D Stephenson, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
X-chromosome inactivation (XCI) patterns in placental tissues of a paternally derived bal t(X;20) caseM S Peñaherrera, S Ma, B Ho Yuen, et al.
Human Reproduction (Oxford, England)|September 20, 2006
Toll-like receptor 4 polymorphisms and idiopathic chromosomally normal miscarriageA F Hirschfeld, R Jiang, W P Robinson, et al.
Clinical Genetics|August 1, 1993
Parental origin of the supernumerary chromosome in trisomy 18X Ya-gang, W P Robinson, R Spiegel, et al.
Human Reproduction (Oxford, England)|October 31, 2003
Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case reportS Ma, S S Tang, B Ho Yuen, et al.
American Journal of Medical Genetics|September 24, 2002
Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnanciesP J Yong, S A Marion, I J Barrett, et al.
Pageof 12