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M Poot

Showing results (101-110 of 104) with videos related to

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American Journal of Medical Genetics. Part A|June 14, 2006
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens, D A Scott, M van Dooren, et al.
Leukemia|March 21, 2012
Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigreesA Buijs, M Poot, S van der Crabben, et al.
Clinical Genetics|October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disordersH M Ozgen, E van Daalen, P F Bolton, et al.
Molecular Psychiatry|November 21, 2012
Common variant at 16p11.2 conferring risk of psychosisS Steinberg, S de Jong, M Mattheisen, et al.
Pageof 11

Showing results (101-110 of 104) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 104 results.
American Journal of Medical Genetics. Part A|June 14, 2006
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens, D A Scott, M van Dooren, et al.
Leukemia|March 21, 2012
Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigreesA Buijs, M Poot, S van der Crabben, et al.
Clinical Genetics|October 2, 2009
Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disordersH M Ozgen, E van Daalen, P F Bolton, et al.
Molecular Psychiatry|November 21, 2012
Common variant at 16p11.2 conferring risk of psychosisS Steinberg, S de Jong, M Mattheisen, et al.
Pageof 11