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I Hansmann

Showing results (111-120 of 129) with videos related to

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American Journal of Medical Genetics|August 3, 2001
Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expressionP Stankiewicz, H Thiele, I Giannakudis, et al.
Human Genetics|January 1, 1983
The genetic significance of accessory bisatellited marker chromosomesP Steinbach, M Djalali, I Hansmann, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 20V Wunderle, C Dib, C Fizames, et al.
American Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVSJ Bernert, I Bartels, G Gatz, et al.
Human Genetics|June 1, 1995
Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyF A Hol, B C Hamel, M P Geurds, et al.
American Journal of Medical Genetics|September 25, 2001
Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 geneP Stankiewicz, J Rujner, C Löffler, et al.
American Journal of Medical Genetics|September 20, 2001
Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locusP Stankiewicz, H Thiele, C Baldermann, et al.
Journal of Medical Genetics|May 23, 1998
Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of XqF Xiang, Z Zhang, A Clarke, et al.
Journal of Medical Genetics|October 1, 1993
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotypeD F Callen, H Eyre, S Lane, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Parental mosaicism of JAG1 mutations in families with Alagille syndromeJ Giannakudis, A Röpke, A Kujat, et al.
Pageof 13

Showing results (111-120 of 129) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics|August 3, 2001
Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expressionP Stankiewicz, H Thiele, I Giannakudis, et al.
Human Genetics|January 1, 1983
The genetic significance of accessory bisatellited marker chromosomesP Steinbach, M Djalali, I Hansmann, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 20V Wunderle, C Dib, C Fizames, et al.
American Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis of the Pallister-Killian mosaic aneuploidy syndrome by CVSJ Bernert, I Bartels, G Gatz, et al.
Human Genetics|June 1, 1995
Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyF A Hol, B C Hamel, M P Geurds, et al.
American Journal of Medical Genetics|September 25, 2001
Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 geneP Stankiewicz, J Rujner, C Löffler, et al.
American Journal of Medical Genetics|September 20, 2001
Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locusP Stankiewicz, H Thiele, C Baldermann, et al.
Journal of Medical Genetics|May 23, 1998
Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of XqF Xiang, Z Zhang, A Clarke, et al.
Journal of Medical Genetics|October 1, 1993
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotypeD F Callen, H Eyre, S Lane, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Parental mosaicism of JAG1 mutations in families with Alagille syndromeJ Giannakudis, A Röpke, A Kujat, et al.
Pageof 13