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S Schuffenhauer

Showing results (41-50 of 45) with videos related to

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European Journal of Human Genetics : EJHG|October 22, 1998
Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, et al.
Human Molecular Genetics|June 13, 1998
Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombinationW P Robinson, B D Kuchinka, F Bernasconi, et al.
Nature|August 10, 2000
GATA3 haplo-insufficiency causes human HDR syndromeH Van Esch, P Groenen, M A Nesbit, 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|November 14, 1997
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative studyA K Ryan, J A Goodship, D I Wilson, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
European Journal of Human Genetics : EJHG|October 22, 1998
Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)S Schuffenhauer, P Lichtner, P Peykar-Derakhshandeh, et al.
Human Molecular Genetics|June 13, 1998
Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombinationW P Robinson, B D Kuchinka, F Bernasconi, et al.
Nature|August 10, 2000
GATA3 haplo-insufficiency causes human HDR syndromeH Van Esch, P Groenen, M A Nesbit, 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|November 14, 1997
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative studyA K Ryan, J A Goodship, D I Wilson, et al.
Pageof 5