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B Grandchamp

Showing results (91-100 of 134) with videos related to

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Leukemia|May 1, 1995
Potential antileukemic effect of gamma delta T cells in acute lymphoblastic leukemiaM Duval, P Yotnda, A Bensussan, et al.
Human Genetics|January 1, 1994
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.
British Journal of Haematology|October 1, 1995
Duodenal expression of NF-E2 in mouse models of altered iron metabolismK B Raja, B Gerard, A T McKie, et al.
Nature Genetics|December 1, 1995
Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataractC Beaumont, P Leneuve, I Devaux, et al.
Blood|November 15, 1995
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1H Cavé, B Gérard, E Martin, et al.
The Journal of Clinical Investigation|February 1, 1986
Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyriaH de Verneuil, B Grandchamp, P H Romeo, et al.
Human Genetics|July 1, 1992
Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyriaH de Verneuil, F Bourgeois, F de Rooij, et al.
Nature Genetics|February 1, 1996
Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyriaR L Lindberg, C Porcher, B Grandchamp, et al.
Human Genetics|March 1, 1993
High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, et al.
American Journal of Human Genetics|June 1, 1997
Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.
Pageof 14

Showing results (91-100 of 134) with videos related to

Sort By:
Pageof 14
Leukemia|May 1, 1995
Potential antileukemic effect of gamma delta T cells in acute lymphoblastic leukemiaM Duval, P Yotnda, A Bensussan, et al.
Human Genetics|January 1, 1994
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.
British Journal of Haematology|October 1, 1995
Duodenal expression of NF-E2 in mouse models of altered iron metabolismK B Raja, B Gerard, A T McKie, et al.
Nature Genetics|December 1, 1995
Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataractC Beaumont, P Leneuve, I Devaux, et al.
Blood|November 15, 1995
Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1H Cavé, B Gérard, E Martin, et al.
The Journal of Clinical Investigation|February 1, 1986
Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyriaH de Verneuil, B Grandchamp, P H Romeo, et al.
Human Genetics|July 1, 1992
Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyriaH de Verneuil, F Bourgeois, F de Rooij, et al.
Nature Genetics|February 1, 1996
Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyriaR L Lindberg, C Porcher, B Grandchamp, et al.
Human Genetics|March 1, 1993
High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, et al.
American Journal of Human Genetics|June 1, 1997
Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.
Pageof 14