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BMC Medical Genetics
|
June 26, 2014
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
Barbara Vona, Indrajit Nanda, Cordula Neuner, et al.
Cells
|
September 23, 2022
Rat Hepatic Stellate Cell Line CFSC-2G: Genetic Markers and Short Tandem Repeat Profile Useful for Cell Line Authentication
Indrajit Nanda, Sarah K Schröder, Claus Steinlein, et al.
Current Biology : CB
|
November 6, 2007
Automictic reproduction in interspecific hybrids of poeciliid fish
Kathrin P Lampert, Dunja K Lamatsch, Petra Fischer, et al.
Molecular Syndromology
|
December 10, 2015
A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment
Michaela A H Hofrichter, Indrajit Nanda, Jens Gräf, et al.
Gene
|
November 8, 2003
Cloning of the dmrt1 gene of Xiphophorus maculatus: dmY/dmrt1Y is not the master sex-determining gene in the platyfish
Anne-Marie Veith, Alexander Froschauer, Cornelia Körting, et al.
Current Biology : CB
|
March 7, 2003
Absence of the candidate male sex-determining gene dmrt1b(Y) of medaka from other fish species
Mariko Kondo, Indrajit Nanda, Ute Hornung, et al.
Cytogenetic and Genome Research
|
April 1, 2015
Co-Occurence of Reciprocal Translocation and COL2A1 Mutation in a Fetus with Severe Skeletal Dysplasia: Implications for Genetic Counseling
Tilman Heinrich, Indrajit Nanda, Monika Rehn, et al.
Aging Cell
|
July 2, 2019
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes
Anna Maierhofer, Julia Flunkert, Junko Oshima, et al.
Cells
|
April 12, 2022
Evolution of the Degenerated Y-Chromosome of the Swamp Guppy, <i>Micropoecilia picta</i>
Indrajit Nanda, Susanne Schories, Ivan Simeonov, et al.
Gene
|
July 30, 2016
CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development
Eberhard Schneider, Marcus Dittrich, Julia Böck, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 59) with videos related to
Sort By:
Page
of 6
BMC Medical Genetics
|
June 26, 2014
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
Barbara Vona, Indrajit Nanda, Cordula Neuner, et al.
Cells
|
September 23, 2022
Rat Hepatic Stellate Cell Line CFSC-2G: Genetic Markers and Short Tandem Repeat Profile Useful for Cell Line Authentication
Indrajit Nanda, Sarah K Schröder, Claus Steinlein, et al.
Current Biology : CB
|
November 6, 2007
Automictic reproduction in interspecific hybrids of poeciliid fish
Kathrin P Lampert, Dunja K Lamatsch, Petra Fischer, et al.
Molecular Syndromology
|
December 10, 2015
A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment
Michaela A H Hofrichter, Indrajit Nanda, Jens Gräf, et al.
Gene
|
November 8, 2003
Cloning of the dmrt1 gene of Xiphophorus maculatus: dmY/dmrt1Y is not the master sex-determining gene in the platyfish
Anne-Marie Veith, Alexander Froschauer, Cornelia Körting, et al.
Current Biology : CB
|
March 7, 2003
Absence of the candidate male sex-determining gene dmrt1b(Y) of medaka from other fish species
Mariko Kondo, Indrajit Nanda, Ute Hornung, et al.
Cytogenetic and Genome Research
|
April 1, 2015
Co-Occurence of Reciprocal Translocation and COL2A1 Mutation in a Fetus with Severe Skeletal Dysplasia: Implications for Genetic Counseling
Tilman Heinrich, Indrajit Nanda, Monika Rehn, et al.
Aging Cell
|
July 2, 2019
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes
Anna Maierhofer, Julia Flunkert, Junko Oshima, et al.
Cells
|
April 12, 2022
Evolution of the Degenerated Y-Chromosome of the Swamp Guppy, <i>Micropoecilia picta</i>
Indrajit Nanda, Susanne Schories, Ivan Simeonov, et al.
Gene
|
July 30, 2016
CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development
Eberhard Schneider, Marcus Dittrich, Julia Böck, et al.
Page
of 6