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I Hansmann

Showing results (91-100 of 129) with videos related to

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Human Genetics|July 1, 1989
The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortionsC Minguillon, B Eiben, S Bähr-Porsch, et al.
Acta Neuropathologica|January 1, 1987
Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardationA Hori, K Tamagawa, S W Eber, et al.
American Journal of Medical Genetics|April 11, 2000
Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7U Hehr, S Dörr, M Hagemann, et al.
Cytogenetics and Cell Genetics|August 31, 2000
Assignment of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridizationM L Ayala-Madrigal, S Doerr, M L Ramírez-Dueñas, et al.
American Journal of Medical Genetics|September 1, 1987
Familial Prader-Willi syndrome with apparently normal chromosomesM Lubinsky, H Zellweger, L Greenswag, et al.
Cytogenetics and Cell Genetics|November 4, 2000
Assignment of karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridizationM L Ayala-Madrigal, S Doerr, M L Ramírez-Dueñas, et al.
Genomics|November 1, 1992
Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH)S Schnittger, V V Rao, U Deutsch, et al.
Human Genetics|June 1, 1991
A sterile male with 45,X0 and a Y;22 translocationJ Arnemann, S Schnittger, G K Hinkel, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Familial mosaicism of del(Y) and inv del(Y)S Röttger, J Pasantes, C Baldermann, et al.
Human Genetics|January 1, 1985
A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequenceJ Schmidtke, J Arnemann, M Schmid, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Human Genetics|July 1, 1989
The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortionsC Minguillon, B Eiben, S Bähr-Porsch, et al.
Acta Neuropathologica|January 1, 1987
Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardationA Hori, K Tamagawa, S W Eber, et al.
American Journal of Medical Genetics|April 11, 2000
Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7U Hehr, S Dörr, M Hagemann, et al.
Cytogenetics and Cell Genetics|August 31, 2000
Assignment of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridizationM L Ayala-Madrigal, S Doerr, M L Ramírez-Dueñas, et al.
American Journal of Medical Genetics|September 1, 1987
Familial Prader-Willi syndrome with apparently normal chromosomesM Lubinsky, H Zellweger, L Greenswag, et al.
Cytogenetics and Cell Genetics|November 4, 2000
Assignment of karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridizationM L Ayala-Madrigal, S Doerr, M L Ramírez-Dueñas, et al.
Genomics|November 1, 1992
Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH)S Schnittger, V V Rao, U Deutsch, et al.
Human Genetics|June 1, 1991
A sterile male with 45,X0 and a Y;22 translocationJ Arnemann, S Schnittger, G K Hinkel, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Familial mosaicism of del(Y) and inv del(Y)S Röttger, J Pasantes, C Baldermann, et al.
Human Genetics|January 1, 1985
A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequenceJ Schmidtke, J Arnemann, M Schmid, et al.
Pageof 13