Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Marianne Volleth

Showing results (11-20 of 42) with videos related to

Pageof 5
Sort By:
American Journal of Medical Genetics. Part A|September 25, 2014
A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndromeIlse Wieland, Denny Schanze, Ina Schanze, et al.
American Journal of Medical Genetics. Part A|May 3, 2006
Intrachromosomal triplication 12p11.22-p12.3 and gonadal mosaicism of partial tetrasomy 12pHeike Eckel, Rainer Wimmer, Marianne Volleth, et al.
Journal of Molecular Endocrinology|June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophyRene Cortese, Florian Eckhardt, Marianne Volleth, et al.
Chromosoma|June 15, 2023
Increased genome size is caused by heterochromatin addition in two non-related bat species, Hesperoptenus doriae and Philetor brachypterus (Vespertilionidae, Chiroptera, Mammalia)Marianne Volleth, Johann Greilhuber, Klaus-Gerhard Heller, et al.
American Journal of Obstetrics and Gynecology|May 1, 2004
Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytesAlbrecht Röpke, Antje-Friederike Pelz, Marianne Volleth, et al.
Genes, Chromosomes & Cancer|July 18, 2006
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11)Ilse Wieland, Petra Muschke, Marianne Volleth, et al.
European Journal of Pediatrics|November 9, 2006
Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTCSibylle Jakubiczka, Thomas Bettecken, Klaus Mohnike, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Genotype/phenotype analysis in a patient with pure and complete trisomy 12pWalter Zumkeller, Marianne Volleth, Petra Muschke, et al.
Clinical Dysmorphology|July 31, 2010
A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardationLoukas Argyriou, Olaf Hiort, Peter Meinecke, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 28, 2007
Karyotype evolution in Rhinolophus bats (Rhinolophidae, Chiroptera) illuminated by cross-species chromosome painting and G-banding comparisonXiuguang Mao, Wenhui Nie, Jinhuan Wang, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|September 25, 2014
A cryptic unbalanced translocation der(4)t(4;17)(p16.1;q25.3) identifies Wittwer syndrome as a variant of Wolf-Hirschhorn syndromeIlse Wieland, Denny Schanze, Ina Schanze, et al.
American Journal of Medical Genetics. Part A|May 3, 2006
Intrachromosomal triplication 12p11.22-p12.3 and gonadal mosaicism of partial tetrasomy 12pHeike Eckel, Rainer Wimmer, Marianne Volleth, et al.
Journal of Molecular Endocrinology|June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophyRene Cortese, Florian Eckhardt, Marianne Volleth, et al.
Chromosoma|June 15, 2023
Increased genome size is caused by heterochromatin addition in two non-related bat species, Hesperoptenus doriae and Philetor brachypterus (Vespertilionidae, Chiroptera, Mammalia)Marianne Volleth, Johann Greilhuber, Klaus-Gerhard Heller, et al.
American Journal of Obstetrics and Gynecology|May 1, 2004
Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytesAlbrecht Röpke, Antje-Friederike Pelz, Marianne Volleth, et al.
Genes, Chromosomes & Cancer|July 18, 2006
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11)Ilse Wieland, Petra Muschke, Marianne Volleth, et al.
European Journal of Pediatrics|November 9, 2006
Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTCSibylle Jakubiczka, Thomas Bettecken, Klaus Mohnike, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Genotype/phenotype analysis in a patient with pure and complete trisomy 12pWalter Zumkeller, Marianne Volleth, Petra Muschke, et al.
Clinical Dysmorphology|July 31, 2010
A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardationLoukas Argyriou, Olaf Hiort, Peter Meinecke, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 28, 2007
Karyotype evolution in Rhinolophus bats (Rhinolophidae, Chiroptera) illuminated by cross-species chromosome painting and G-banding comparisonXiuguang Mao, Wenhui Nie, Jinhuan Wang, et al.
Pageof 5