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C Weemaes

Showing results (11-20 of 13) with videos related to

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American Journal of Human Genetics|June 1, 1997
Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24S Matsuura, C Weemaes, D Smeets, et al.
Human Mutation|January 11, 2000
Genetic variation in ICF syndrome: evidence for genetic heterogeneityC Wijmenga, R S Hansen, G Gimelli, et al.
Clinical Genetics|January 28, 2017
Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2M L van den Boogaard, P E Thijssen, C Aytekin, et al.
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Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
American Journal of Human Genetics|June 1, 1997
Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24S Matsuura, C Weemaes, D Smeets, et al.
Human Mutation|January 11, 2000
Genetic variation in ICF syndrome: evidence for genetic heterogeneityC Wijmenga, R S Hansen, G Gimelli, et al.
Clinical Genetics|January 28, 2017
Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2M L van den Boogaard, P E Thijssen, C Aytekin, et al.
Pageof 2