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Gaby Lederer

Showing results (1-10 of 5) with videos related to

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Mutagenesis|November 19, 2002
Multicolor FISH in two and three dimensions for clastogenic analysesChristine Maierhofer, Isabell Jentsch, Gaby Lederer, et al.
Cancer Research|December 3, 2004
Analysis of gene expression patterns and chromosomal changes associated with agingJochen B Geigl, Sabine Langer, Simone Barwisch, et al.
American Journal of Medical Genetics. Part A|August 14, 2009
Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterizationMaja Hempel, Nuria Rivera Brugués, Janine Wagenstaller, et al.
American Journal of Medical Genetics. Part A|March 9, 2006
Delineation of a 2q deletion in a girl with dysmorphic features and epilepsySabine Langer, Jochen B Geigl, Janine Wagenstaller, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndromeWalter Bonfig, Nabeel J M Salem, Katrin Heiliger, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Mutagenesis|November 19, 2002
Multicolor FISH in two and three dimensions for clastogenic analysesChristine Maierhofer, Isabell Jentsch, Gaby Lederer, et al.
Cancer Research|December 3, 2004
Analysis of gene expression patterns and chromosomal changes associated with agingJochen B Geigl, Sabine Langer, Simone Barwisch, et al.
American Journal of Medical Genetics. Part A|August 14, 2009
Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterizationMaja Hempel, Nuria Rivera Brugués, Janine Wagenstaller, et al.
American Journal of Medical Genetics. Part A|March 9, 2006
Delineation of a 2q deletion in a girl with dysmorphic features and epilepsySabine Langer, Jochen B Geigl, Janine Wagenstaller, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndromeWalter Bonfig, Nabeel J M Salem, Katrin Heiliger, et al.
Pageof 1