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Prenatal Diagnosis
|
March 28, 2007
Syndromic encephalocele in a fetal case with a 1p35-pter deletion and a 14q32-qter duplication inherited from a maternal balanced translocation
C Thauvin-Robinet, P Callier, N Laurent, et al.
American Journal of Medical Genetics. Part A
|
August 8, 2006
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization
P Callier, L Faivre, N Marle, et al.
Leukemia
|
July 1, 1991
P-glycoprotein expression and in vitro reversion of doxorubicin resistance by verapamil in clinical specimens from acute leukaemia and myeloma
E Solary, J M Bidan, F Calvo, et al.
American Journal of Human Genetics
|
May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region
N Dahl, L J Hu, M Chery, et al.
American Journal of Medical Genetics. Part A
|
August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
P Callier, L Faivre, V Cusin, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1988
Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12)
C Turc-Carel, A Aurias, F Mugneret, et al.
Annales De Genetique
|
January 1, 1992
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases
M Poissonnier, C Turleau, M Olivier-Martin, et al.
Cancer Genetics and Cytogenetics
|
August 1, 1997
Translocation 1;19 in two brain tumors
A M Vagner-Capodano, F Mugneret, H Zattara-Cannoni, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 10, 2001
Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia
T Mercher, M B Coniat, R Monni, et al.
Leukemia
|
January 22, 1998
Immunophenotypic patterns and cytogenetic anomalies in acute non-lymphoblastic leukemia subtypes: a prospective study of 432 patients
R O Casasnovas, L Campos, F Mugneret, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 66) with videos related to
Sort By:
Page
of 7
Prenatal Diagnosis
|
March 28, 2007
Syndromic encephalocele in a fetal case with a 1p35-pter deletion and a 14q32-qter duplication inherited from a maternal balanced translocation
C Thauvin-Robinet, P Callier, N Laurent, et al.
American Journal of Medical Genetics. Part A
|
August 8, 2006
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization
P Callier, L Faivre, N Marle, et al.
Leukemia
|
July 1, 1991
P-glycoprotein expression and in vitro reversion of doxorubicin resistance by verapamil in clinical specimens from acute leukaemia and myeloma
E Solary, J M Bidan, F Calvo, et al.
American Journal of Human Genetics
|
May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region
N Dahl, L J Hu, M Chery, et al.
American Journal of Medical Genetics. Part A
|
August 2, 2005
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
P Callier, L Faivre, V Cusin, et al.
Cancer Genetics and Cytogenetics
|
June 1, 1988
Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12)
C Turc-Carel, A Aurias, F Mugneret, et al.
Annales De Genetique
|
January 1, 1992
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases
M Poissonnier, C Turleau, M Olivier-Martin, et al.
Cancer Genetics and Cytogenetics
|
August 1, 1997
Translocation 1;19 in two brain tumors
A M Vagner-Capodano, F Mugneret, H Zattara-Cannoni, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 10, 2001
Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia
T Mercher, M B Coniat, R Monni, et al.
Leukemia
|
January 22, 1998
Immunophenotypic patterns and cytogenetic anomalies in acute non-lymphoblastic leukemia subtypes: a prospective study of 432 patients
R O Casasnovas, L Campos, F Mugneret, et al.
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of 7