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B Zabel

Showing results (61-70 of 120) with videos related to

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Prenatal Diagnosis|May 1, 1996
Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorptionM G Martín, E Turk, C Kerner, et al.
Cytogenetics and Cell Genetics|August 31, 2001
Genomic imbalances in 61 renal cancers from the proximal tubulus detected by comparative genomic hybridizationD Reutzel, M Mende, S Naumann, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1989
[Simultaneous double fluorescence flow cytometry of lysed whole blood for prenatal diagnosis of combined immunodeficiency]O Schofer, F Zepp, E März, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primatesZ Shan, B Zabel, U Trautmann, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
A familial case of achondrogenesis type II caused by a dominant COL2A1 mutation and "patchy" expression in the mosaic fatherF Forzano, M Lituania, A Viassolo, et al.
The Journal of Experimental Medicine|December 1, 1994
One gene, two transcripts: isolation of an alternative transcript encoding for the autoantigen La/SS-B from a cDNA library of a patient with primary Sjögrens' syndromeH Tröster, T E Metzger, I Semsei, et al.
American Journal of Medical Genetics|September 1, 1992
Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type IIM Beck, C Steglich, B Zabel, et al.
Journal of Medical Genetics|September 19, 2000
Equal expression of typ X collagen mRNA fom mutant and wild type COL10A1 alleles in growth plate cartilage from a patient with metaphyseal chondrodysplasia type SchmidC A Gregory, B Zabel, M E Grant, et al.
Journal of Medical Genetics|May 20, 2000
Clinical variability of Stickler syndrome with a COL2A1 haploinsufficiency mutation: implications for genetic counsellingJ Faber, A Winterpacht, B Zabel, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 20, 1999
[Molecular genetic study of the PAX6 gene in aniridia patients]M Wolf, B Zabel, B Lorenz, et al.
Pageof 12

Showing results (61-70 of 120) with videos related to

Sort By:
Pageof 12
Prenatal Diagnosis|May 1, 1996
Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorptionM G Martín, E Turk, C Kerner, et al.
Cytogenetics and Cell Genetics|August 31, 2001
Genomic imbalances in 61 renal cancers from the proximal tubulus detected by comparative genomic hybridizationD Reutzel, M Mende, S Naumann, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1989
[Simultaneous double fluorescence flow cytometry of lysed whole blood for prenatal diagnosis of combined immunodeficiency]O Schofer, F Zepp, E März, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primatesZ Shan, B Zabel, U Trautmann, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
A familial case of achondrogenesis type II caused by a dominant COL2A1 mutation and "patchy" expression in the mosaic fatherF Forzano, M Lituania, A Viassolo, et al.
The Journal of Experimental Medicine|December 1, 1994
One gene, two transcripts: isolation of an alternative transcript encoding for the autoantigen La/SS-B from a cDNA library of a patient with primary Sjögrens' syndromeH Tröster, T E Metzger, I Semsei, et al.
American Journal of Medical Genetics|September 1, 1992
Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type IIM Beck, C Steglich, B Zabel, et al.
Journal of Medical Genetics|September 19, 2000
Equal expression of typ X collagen mRNA fom mutant and wild type COL10A1 alleles in growth plate cartilage from a patient with metaphyseal chondrodysplasia type SchmidC A Gregory, B Zabel, M E Grant, et al.
Journal of Medical Genetics|May 20, 2000
Clinical variability of Stickler syndrome with a COL2A1 haploinsufficiency mutation: implications for genetic counsellingJ Faber, A Winterpacht, B Zabel, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 20, 1999
[Molecular genetic study of the PAX6 gene in aniridia patients]M Wolf, B Zabel, B Lorenz, et al.
Pageof 12