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Showing results (11-20 of 16) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1996
Isochromosome 18p results from maternal meiosis II nondisjunctionD Kotzot, G Bundscherer, F Bernasconi, et al.
Annals of Neurology|July 14, 2000
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotypeC Klein, P P Pramstaller, B Kis, et al.
Journal of Medical Genetics|November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formationE Rossi, M Riegel, J Messa, et al.
Journal of Medical Genetics|April 4, 2000
Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplicationsD Kotzot, M J Martinez, G Bagci, et al.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
European Journal of Human Genetics : EJHG|January 1, 1996
Isochromosome 18p results from maternal meiosis II nondisjunctionD Kotzot, G Bundscherer, F Bernasconi, et al.
Annals of Neurology|July 14, 2000
Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotypeC Klein, P P Pramstaller, B Kis, et al.
Journal of Medical Genetics|November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formationE Rossi, M Riegel, J Messa, et al.
Journal of Medical Genetics|April 4, 2000
Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplicationsD Kotzot, M J Martinez, G Bagci, et al.
Journal of Medical Genetics|June 27, 2001
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformationsE Rossi, F Piccini, M Zollino, et al.
American Journal of Human Genetics|September 6, 2001
CNGA3 mutations in hereditary cone photoreceptor disordersB Wissinger, D Gamer, H Jägle, et al.
Pageof 2