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M F Portnoï

Showing results (1-10 of 14) with videos related to

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Molecular and Cellular Endocrinology|January 28, 1999
Genes and premature ovarian failureS Christin-Maitre, C Vasseur, M F Portnoï, et al.
Obstetrics and Gynecology|July 1, 1988
Karyotypes of 1142 couples with recurrent abortionM F Portnoï, N Joye, J van den Akker, et al.
Leukemia & Lymphoma|September 6, 2007
Simultaneous regression of Philadelphia chromosome and multiple nonrecurrent clonal chromosomal abnormalities with imatinib mesylate in a patient autografted 22 years before for chronic myelogenous leukemiaJ Van Den Akker, P Coppo, M F Portnoï, et al.
Bone Marrow Transplantation|August 26, 1998
Unrelated mismatched cord blood transplantation in patients with hematological malignancies: a single institution experienceJ P Laporte, S Lesage, M F Portnoï, et al.
Prenatal Diagnosis|June 21, 2005
Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotypeM-P Beaujard, J-M Jouannic, B Bessières, et al.
Journal of Medical Genetics|March 21, 1998
Prenatal diagnosis by FISH of a 22q11 deletion in two familiesM F Portnoï, N Joyé, M Gonzales, et al.
Annales De Genetique|September 1, 2004
Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalisN Bouayed Abdelmoula, M F Portnoï, A Amouri, et al.
Annales De Genetique|January 1, 1995
[Translocation t(6;9;8)(p23;q34;q22) in acute myeloid leukemia: Contribution of fluorescence in situ hybridization]J van den Akker, C Pérot, M F Portnoï, et al.
Human Molecular Genetics|November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctataD Weil, M F Portnoï, J Levilliers, et al.
American Journal of Medical Genetics|August 3, 2001
Pierre Robin sequence and interstitial deletion 2q32.3-q33.2C Houdayer, M F Portnoï, F Vialard, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Molecular and Cellular Endocrinology|January 28, 1999
Genes and premature ovarian failureS Christin-Maitre, C Vasseur, M F Portnoï, et al.
Obstetrics and Gynecology|July 1, 1988
Karyotypes of 1142 couples with recurrent abortionM F Portnoï, N Joye, J van den Akker, et al.
Leukemia & Lymphoma|September 6, 2007
Simultaneous regression of Philadelphia chromosome and multiple nonrecurrent clonal chromosomal abnormalities with imatinib mesylate in a patient autografted 22 years before for chronic myelogenous leukemiaJ Van Den Akker, P Coppo, M F Portnoï, et al.
Bone Marrow Transplantation|August 26, 1998
Unrelated mismatched cord blood transplantation in patients with hematological malignancies: a single institution experienceJ P Laporte, S Lesage, M F Portnoï, et al.
Prenatal Diagnosis|June 21, 2005
Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotypeM-P Beaujard, J-M Jouannic, B Bessières, et al.
Journal of Medical Genetics|March 21, 1998
Prenatal diagnosis by FISH of a 22q11 deletion in two familiesM F Portnoï, N Joyé, M Gonzales, et al.
Annales De Genetique|September 1, 2004
Turner syndrome female with a small ring X chromosome lacking the XIST, an unexpectedly mild phenotype and an atypical association with alopecia universalisN Bouayed Abdelmoula, M F Portnoï, A Amouri, et al.
Annales De Genetique|January 1, 1995
[Translocation t(6;9;8)(p23;q34;q22) in acute myeloid leukemia: Contribution of fluorescence in situ hybridization]J van den Akker, C Pérot, M F Portnoï, et al.
Human Molecular Genetics|November 1, 1993
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctataD Weil, M F Portnoï, J Levilliers, et al.
American Journal of Medical Genetics|August 3, 2001
Pierre Robin sequence and interstitial deletion 2q32.3-q33.2C Houdayer, M F Portnoï, F Vialard, et al.
Pageof 2