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I Hansmann

Showing results (71-80 of 129) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1992
The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridizationV V Rao, C Löffler, J Battey, et al.
American Journal of Medical Genetics|June 1, 1984
Developmental pathogenesis of chromosome disorders: report on two newly recognized signs of Down syndromeU Langenbeck, E Blum, C Wilkert-Walter, et al.
Human Genetics|January 1, 1981
H-Y antigen in Turner's syndrome patients with different sex chromosome constitutionsW Engel, B Klemme, H D Probeck, et al.
Clinical Genetics|December 1, 1978
Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatinH J Gebauer, B Stumpf, I Hansmann, et al.
Cytogenetics and Cell Genetics|January 1, 1991
The gene for human growth hormone-releasing factor (GHRF) maps to or near chromosome 20p12V V Rao, C Löffler, S Schnittger, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Epsilon subunit gene of F(1)F(0)-ATP synthase (ATP5E) on human chromosome 20q13.2-->q13.3 localizes between D20S171 and GNAS1C Gross, S Kussmann, A Hehr, et al.
Biologisches Zentralblatt|September 28, 2018
MECHANISMS OF NONDISJUNCTION AND IMPLICATIONS FOR TESTING ANEUGENSI Hansmann, F Beermann, E Hummler, et al.
Clinical Genetics|January 1, 1988
Partial deletion of 4p in fetal cells not present in chorionic villiB Eiben, M Leipoldt, I Schübbe, et al.
American Journal of Medical Genetics|December 1, 1989
Down syndrome at birth not detected by first-trimester chorionic villus samplingI Bartels, I Hansmann, U Holland, et al.
Human Genetics|October 1, 1989
Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)S Schnittger, C Höfers, P Heidemann, et al.
Pageof 13

Showing results (71-80 of 129) with videos related to

Sort By:
Pageof 13
Cytogenetics and Cell Genetics|January 1, 1992
The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridizationV V Rao, C Löffler, J Battey, et al.
American Journal of Medical Genetics|June 1, 1984
Developmental pathogenesis of chromosome disorders: report on two newly recognized signs of Down syndromeU Langenbeck, E Blum, C Wilkert-Walter, et al.
Human Genetics|January 1, 1981
H-Y antigen in Turner's syndrome patients with different sex chromosome constitutionsW Engel, B Klemme, H D Probeck, et al.
Clinical Genetics|December 1, 1978
Cri-du-chat syndrome in a child with a 5/15 translocation and interstitial centromeric heterochromatinH J Gebauer, B Stumpf, I Hansmann, et al.
Cytogenetics and Cell Genetics|January 1, 1991
The gene for human growth hormone-releasing factor (GHRF) maps to or near chromosome 20p12V V Rao, C Löffler, S Schnittger, et al.
Cytogenetics and Cell Genetics|February 15, 2001
Epsilon subunit gene of F(1)F(0)-ATP synthase (ATP5E) on human chromosome 20q13.2-->q13.3 localizes between D20S171 and GNAS1C Gross, S Kussmann, A Hehr, et al.
Biologisches Zentralblatt|September 28, 2018
MECHANISMS OF NONDISJUNCTION AND IMPLICATIONS FOR TESTING ANEUGENSI Hansmann, F Beermann, E Hummler, et al.
Clinical Genetics|January 1, 1988
Partial deletion of 4p in fetal cells not present in chorionic villiB Eiben, M Leipoldt, I Schübbe, et al.
American Journal of Medical Genetics|December 1, 1989
Down syndrome at birth not detected by first-trimester chorionic villus samplingI Bartels, I Hansmann, U Holland, et al.
Human Genetics|October 1, 1989
Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)S Schnittger, C Höfers, P Heidemann, et al.
Pageof 13