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Christine Fauth

Showing results (1-10 of 61) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 23, 2026
Christine Fauth, Sarah Verheyen
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 27, 2026
Patricia Döttelmayer, Christine Fauth
Prenatal Diagnosis|October 24, 2017
Comment on "Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome"Christine Fauth, Annick Toutain
American Journal of Medical Genetics. Part A|March 29, 2014
FKBP14-related Ehlers-Danlos syndrome: expansion of the phenotype to include vascular complicationsMitzi L Murray, Margaret Yang, Christine Fauth, et al.
Clinical Case Reports|February 5, 2024
Treatment of psychiatric comorbidities and interaction patterns in Coffin-Siris syndrome: A case report of a 4-year-old girlAnn-Christin Jahnke-Majorkovits, Christine Fauth, Manuela Gander, et al.
European Journal of Medical Genetics|August 19, 2008
The changing phenotype in diploid/triploid mosaicism may mimic genetic syndromes with aberrant genomic imprinting: follow up in a 14-year-old girlOlaf Rittinger, Gabriela Kronberger, Andrea Pfeifenberger, et al.
Mutagenesis|November 19, 2002
Multicolor FISH in two and three dimensions for clastogenic analysesChristine Maierhofer, Isabell Jentsch, Gaby Lederer, et al.
American Journal of Medical Genetics. Part A|February 28, 2008
Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy womanMartina Höckner, Barbara Utermann, Martin Erdel, et al.
European Journal of Human Genetics : EJHG|December 9, 2004
Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) geneThomas Eggermann, Klaus Zerres, Dirk Anhuf, et al.
Genes, Chromosomes & Cancer|June 10, 2004
Order of genetic events is critical determinant of aberrations in chromosome count and structureChristine Fauth, Michael J O'Hare, Gabi Lederer, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 23, 2026
Christine Fauth, Sarah Verheyen
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|April 27, 2026
Patricia Döttelmayer, Christine Fauth
Prenatal Diagnosis|October 24, 2017
Comment on "Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome"Christine Fauth, Annick Toutain
American Journal of Medical Genetics. Part A|March 29, 2014
FKBP14-related Ehlers-Danlos syndrome: expansion of the phenotype to include vascular complicationsMitzi L Murray, Margaret Yang, Christine Fauth, et al.
Clinical Case Reports|February 5, 2024
Treatment of psychiatric comorbidities and interaction patterns in Coffin-Siris syndrome: A case report of a 4-year-old girlAnn-Christin Jahnke-Majorkovits, Christine Fauth, Manuela Gander, et al.
European Journal of Medical Genetics|August 19, 2008
The changing phenotype in diploid/triploid mosaicism may mimic genetic syndromes with aberrant genomic imprinting: follow up in a 14-year-old girlOlaf Rittinger, Gabriela Kronberger, Andrea Pfeifenberger, et al.
Mutagenesis|November 19, 2002
Multicolor FISH in two and three dimensions for clastogenic analysesChristine Maierhofer, Isabell Jentsch, Gaby Lederer, et al.
American Journal of Medical Genetics. Part A|February 28, 2008
Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy womanMartina Höckner, Barbara Utermann, Martin Erdel, et al.
European Journal of Human Genetics : EJHG|December 9, 2004
Somatic mosaicism for a heterozygous deletion of the survival motor neuron (SMN1) geneThomas Eggermann, Klaus Zerres, Dirk Anhuf, et al.
Genes, Chromosomes & Cancer|June 10, 2004
Order of genetic events is critical determinant of aberrations in chromosome count and structureChristine Fauth, Michael J O'Hare, Gabi Lederer, et al.
Pageof 7