E Petek|P M Kroisel|K Wagner - JoVE Visualize

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Clinical Genetics|December 8, 1998

Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephalyE Petek, P M Kroisel, K Wagner

American Journal of Medical Genetics|August 3, 2001

Phenotype of five patients with Greig syndrome and microdeletion of 7p13P M Kroisel, E Petek, K Wagner

Genetic Counseling (Geneva, Switzerland)|May 23, 2002

Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical regionM Tschernigg, E Petek, K Wagner, et al.

Cytogenetic and Genome Research|November 20, 2002

Chromosomal localization and genomic organization of the human Linker for Activation of T cells (LAT) geneC Windpassinger, P M Kroisel, K Wagner, et al.

Clinical Dysmorphology|January 29, 2000

Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISHE Petek, G Köstl, I Mutz, et al.

American Journal of Medical Genetics|December 26, 2001

Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndromeW Emberger, E Petek, P M Kroisel, et al.

Genetic Counseling (Geneva, Switzerland)|November 6, 2002

Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13)M Tschernigg, E Petek, A Leonhardtsberger, et al.

American Journal of Medical Genetics|May 20, 1999

Mosaicism in a fragile X male including a de novo deletion in the FMR1 geneE Petek, P M Kroisel, M Schuster, et al.

Genetic Counseling (Geneva, Switzerland)|May 23, 2007

Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotypeM Mach, C Windpassinger, K Wagner, et al.

Prenatal Diagnosis|March 31, 2000

Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformationE Petek, K Wagner, H Steiner, et al.

Pageof 157

Showing results (1-10 of 1,567) with videos related to

Sort By:

Pageof 157

Clinical Genetics|December 8, 1998

Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephalyE Petek, P M Kroisel, K Wagner

American Journal of Medical Genetics|August 3, 2001

Phenotype of five patients with Greig syndrome and microdeletion of 7p13P M Kroisel, E Petek, K Wagner

Genetic Counseling (Geneva, Switzerland)|May 23, 2002

Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical regionM Tschernigg, E Petek, K Wagner, et al.

Cytogenetic and Genome Research|November 20, 2002

Chromosomal localization and genomic organization of the human Linker for Activation of T cells (LAT) geneC Windpassinger, P M Kroisel, K Wagner, et al.

Clinical Dysmorphology|January 29, 2000

Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISHE Petek, G Köstl, I Mutz, et al.

American Journal of Medical Genetics|December 26, 2001

Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndromeW Emberger, E Petek, P M Kroisel, et al.

Genetic Counseling (Geneva, Switzerland)|November 6, 2002

Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13)M Tschernigg, E Petek, A Leonhardtsberger, et al.

American Journal of Medical Genetics|May 20, 1999

Mosaicism in a fragile X male including a de novo deletion in the FMR1 geneE Petek, P M Kroisel, M Schuster, et al.

Genetic Counseling (Geneva, Switzerland)|May 23, 2007

Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotypeM Mach, C Windpassinger, K Wagner, et al.

Prenatal Diagnosis|March 31, 2000

Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformationE Petek, K Wagner, H Steiner, et al.

Pageof 157