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T Lyngbye

Showing results (21-30 of 25) with videos related to

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Acta Paediatrica Scandinavica|March 1, 1990
Learning disabilities in children: significance of low-level lead-exposure and confounding factorsT Lyngbye, O N Hansen, A Trillingsgaard, et al.
Neurotoxicology and Teratology|May 1, 1989
A neuropsychological study of children with elevated dentine lead level: assessment of the effect of lead in different socio-economic groupsO N Hansen, A Trillingsgaard, I Beese, et al.
Human Genetics|October 19, 1978
Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndromeK B Nielsen, H Dyggve, U Friedrich, et al.
Human Genetics|August 2, 2001
Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridiaK Grønskov, J H Olsen, A Sand, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Tetrasomy 18p de novo: parental origin and different mechanisms of formationM Bugge, E Blennow, U Friedrich, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Acta Paediatrica Scandinavica|March 1, 1990
Learning disabilities in children: significance of low-level lead-exposure and confounding factorsT Lyngbye, O N Hansen, A Trillingsgaard, et al.
Neurotoxicology and Teratology|May 1, 1989
A neuropsychological study of children with elevated dentine lead level: assessment of the effect of lead in different socio-economic groupsO N Hansen, A Trillingsgaard, I Beese, et al.
Human Genetics|October 19, 1978
Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndromeK B Nielsen, H Dyggve, U Friedrich, et al.
Human Genetics|August 2, 2001
Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridiaK Grønskov, J H Olsen, A Sand, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Tetrasomy 18p de novo: parental origin and different mechanisms of formationM Bugge, E Blennow, U Friedrich, et al.
Pageof 3