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M F Croquette

Showing results (11-20 of 48) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[ Head and truncal abnormalities and secondary clinical aspects of 22q11 microdeletion. A series of 111 patients]G M Brevière, M F Croquette, B Delobel, et al.
Nouvelle Revue Francaise D'Hematologie|November 1, 1970
[A peculiar form of granulocytic leukemia in the male: prolonged development and the presence of the Philadelphia chromosome, with the loss of Y chromosome in the myeloid cells (apropos of 3 cases)]F Bauters, M F Croquette, Y Delmas-Marsalet, et al.
Human Genetics|January 1, 1986
New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct(14;14) and inv(14)A Aurias, M F Croquette, J P Nuyts, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 9, 1999
Identification of the gene-richest bands in human prometaphase chromosomesS Saccone, C Federico, I Solovei, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 16, 1998
[Smith-Magenis syndrome]M O Livet, A Moncla, B Delobel, et al.
Journal De Genetique Humaine|June 1, 1989
[Lethal polymalformative syndrome with 13q deletion secondary to a maternal X; 13 translocation]G Vittu, M F Croquette, A Donney, et al.
Journal of Clinical Pathology|February 28, 2002
Renal oncocytoma with a novel chromosomal rearrangement, der(13)t(13;16)(p11;p11), associated with a renal cell carcinomaX Leroy, E Leteurtre, P H Mahe, et al.
Andrologia|May 1, 1995
XY-quadrivalent association and sterility in a man carrier of a reciprocal autosomal translocation involving the whole arm of an acrocentric chromosome t(2;15)(q21.3;cen)W R Yu, O Gabriel-Robez, M F Croquette, et al.
American Journal of Medical Genetics|December 8, 1998
Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestationsB Delobel, V Delannoy, G Pini, et al.
Annales De Genetique|January 1, 1996
Synaptic behaviour of sex chromosome in two XYY menO Gabriel-Robez, B Delobel, M F Croquette, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

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Pageof 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[ Head and truncal abnormalities and secondary clinical aspects of 22q11 microdeletion. A series of 111 patients]G M Brevière, M F Croquette, B Delobel, et al.
Nouvelle Revue Francaise D'Hematologie|November 1, 1970
[A peculiar form of granulocytic leukemia in the male: prolonged development and the presence of the Philadelphia chromosome, with the loss of Y chromosome in the myeloid cells (apropos of 3 cases)]F Bauters, M F Croquette, Y Delmas-Marsalet, et al.
Human Genetics|January 1, 1986
New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct(14;14) and inv(14)A Aurias, M F Croquette, J P Nuyts, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 9, 1999
Identification of the gene-richest bands in human prometaphase chromosomesS Saccone, C Federico, I Solovei, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 16, 1998
[Smith-Magenis syndrome]M O Livet, A Moncla, B Delobel, et al.
Journal De Genetique Humaine|June 1, 1989
[Lethal polymalformative syndrome with 13q deletion secondary to a maternal X; 13 translocation]G Vittu, M F Croquette, A Donney, et al.
Journal of Clinical Pathology|February 28, 2002
Renal oncocytoma with a novel chromosomal rearrangement, der(13)t(13;16)(p11;p11), associated with a renal cell carcinomaX Leroy, E Leteurtre, P H Mahe, et al.
Andrologia|May 1, 1995
XY-quadrivalent association and sterility in a man carrier of a reciprocal autosomal translocation involving the whole arm of an acrocentric chromosome t(2;15)(q21.3;cen)W R Yu, O Gabriel-Robez, M F Croquette, et al.
American Journal of Medical Genetics|December 8, 1998
Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestationsB Delobel, V Delannoy, G Pini, et al.
Annales De Genetique|January 1, 1996
Synaptic behaviour of sex chromosome in two XYY menO Gabriel-Robez, B Delobel, M F Croquette, et al.
Pageof 5