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B De Graaf

Showing results (61-70 of 64) with videos related to

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American Journal of Medical Genetics. Part A|July 29, 2003
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-upA K Mostert, P F Dijkstra, B R H Jansen, et al.
Brain : a Journal of Neurology|September 26, 2001
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22S M Rosso, W Kamphorst, B de Graaf, et al.
Human Reproduction (Oxford, England)|August 12, 2008
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locusR A Oldenburg, M F van Dooren, B de Graaf, et al.
Journal of Medical Genetics|July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3A S Brooks, P A Leegwater, G M Burzynski, et al.
Pageof 7

Showing results (61-70 of 64) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 64 results.
American Journal of Medical Genetics. Part A|July 29, 2003
Familial multiple epiphyseal dysplasia due to a matrilin-3 mutation: further delineation of the phenotype including 40 years follow-upA K Mostert, P F Dijkstra, B R H Jansen, et al.
Brain : a Journal of Neurology|September 26, 2001
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22S M Rosso, W Kamphorst, B de Graaf, et al.
Human Reproduction (Oxford, England)|August 12, 2008
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locusR A Oldenburg, M F van Dooren, B de Graaf, et al.
Journal of Medical Genetics|July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3A S Brooks, P A Leegwater, G M Burzynski, et al.
Pageof 7