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T W Hustinx

Showing results (41-50 of 47) with videos related to

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Acta Paediatrica Scandinavica|July 1, 1981
A new chromosomal instability disorder: the Nijmegen breakage syndromeC M Weemaes, T W Hustinx, J M Scheres, et al.
Brain & Development|January 1, 1983
Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncleW O Renier, F J Gabreëls, T W Hustinx, et al.
Clinical Genetics|August 1, 1977
Bloom's syndrome in two Dutch familiesT W Hustinx, B G Ter Haar, J M Scheres, et al.
Journal of Mental Deficiency Research|March 1, 1983
The Martin-Bell syndrome: a psychological, logopaedic and cytogenetic study of two affected brothersW O Renier, D F Smeets, J M Scheres, et al.
Clinical Genetics|October 1, 1983
Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibsW O Renier, F A Nabben, T W Hustinx, et al.
Acta Neuropathologica|January 1, 1981
Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousinsW O Renier, F J Gabreëls, T W Hustinx, et al.
Human Genetics|June 1, 1990
Paracentric inversion inv(11)(q21q23) in The NetherlandsK Madan, M H Pieters, L P Kuyt, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Acta Paediatrica Scandinavica|July 1, 1981
A new chromosomal instability disorder: the Nijmegen breakage syndromeC M Weemaes, T W Hustinx, J M Scheres, et al.
Brain & Development|January 1, 1983
Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncleW O Renier, F J Gabreëls, T W Hustinx, et al.
Clinical Genetics|August 1, 1977
Bloom's syndrome in two Dutch familiesT W Hustinx, B G Ter Haar, J M Scheres, et al.
Journal of Mental Deficiency Research|March 1, 1983
The Martin-Bell syndrome: a psychological, logopaedic and cytogenetic study of two affected brothersW O Renier, D F Smeets, J M Scheres, et al.
Clinical Genetics|October 1, 1983
Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibsW O Renier, F A Nabben, T W Hustinx, et al.
Acta Neuropathologica|January 1, 1981
Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousinsW O Renier, F J Gabreëls, T W Hustinx, et al.
Human Genetics|June 1, 1990
Paracentric inversion inv(11)(q21q23) in The NetherlandsK Madan, M H Pieters, L P Kuyt, et al.
Pageof 5