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M Holvoet

Showing results (11-20 of 22) with videos related to

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Journal of Medical Genetics|November 10, 2000
Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1T J De Ravel, G Matthijs, M Holvoet, et al.
American Journal of Medical Genetics|March 4, 2000
Cri du chat syndrome: changing phenotype in older patientsG J Van Buggenhout, E Pijkels, M Holvoet, et al.
American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
Clinical Genetics|June 1, 1991
A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardationM Haspeslagh, J P Fryns, M Holvoet, et al.
Clinical Genetics|May 21, 2004
ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarismH Van Esch, K Poirier, F de Zegher, et al.
Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, et al.
Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.
Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|November 10, 2000
Idiopathic multicentric osteolysis presents early and is not linked to chromosome 18q21.1T J De Ravel, G Matthijs, M Holvoet, et al.
American Journal of Medical Genetics|March 4, 2000
Cri du chat syndrome: changing phenotype in older patientsG J Van Buggenhout, E Pijkels, M Holvoet, et al.
American Journal of Medical Genetics|February 7, 1998
Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50)S Claes, A Vogels, M Holvoet, et al.
American Journal of Medical Genetics|July 9, 1999
Regional localization of a gene for nonspecific XLMR to Xp11.3-p11. 23 (MRX51) and tentative localization of an MRX gene to Xq23-q26.1S Claes, P Volcke, K Devriendt, et al.
Clinical Genetics|June 1, 1991
A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardationM Haspeslagh, J P Fryns, M Holvoet, et al.
Clinical Genetics|May 21, 2004
ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarismH Van Esch, K Poirier, F de Zegher, et al.
Annales De Genetique|February 13, 2001
Cryptic translocation t(5;18) in familial mental retardationA Vogels, K Devriendt, J R Vermeesch, et al.
Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.
Clinical Genetics|June 11, 1999
Partial DiGeorge syndrome in two patients with a 10p rearrangementH Van Esch, P Groenen, S Daw, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
Pageof 3