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Results of search for 'au:"Gregoire, M J"', page 1 of 2
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Authors
Aymard, J P
Berger, R
Birnbaum, D
Bonnet, C
Bordigoni, P
Buisine, J
Béné, M C
Chery, M
Dastugue, N
Gilgenkrantz, S
Gregoire, M J
Grégoire, M J
Grégoire, M-J
Hagemeijer, A
Jonveaux, P
Kessler, M
Lafage-Pochitaloff, M
Lederlin, P
Pernot, C
Streiff, F
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Topics
Abnormalities, Multiple
Adolescent
Adult
Aged
Child
Child, Preschool
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosomes, Human, 1-3
Chromosomes, Human, 6-12 and X
Female
Humans
Infant
Karyotyping
Male
Middle Aged
Pedigree
Translocation, Genetic
genetics
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English
French
Your search returned 39 results.
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1.
[Action of 5-bromodeoxyuridine as a function of time on the aspect of chromosomes. Attempt at interpretation].
[electronic resource]
by
Gilgenkrantz, S
Gregoire, M J
Streiff, F
Producer:
19770224
In:
Comptes rendus des seances de la Societe de biologie et de ses filiales
vol. 170
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2.
[Cytogenetic studies in spontaneous abortions].
[electronic resource]
by
Gilgenkrantz, S
Gregoire, M J
Streiff, F
Producer:
19770512
In:
Bulletin de l'Association des anatomistes
vol. 60
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3.
[Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families].
[electronic resource]
by
Gilgenkrantz, S
Boué, J
Grégoire, M J
Tejada, I
Producer:
19841102
In:
Journal de genetique humaine
vol. 32
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4.
Proximal trisomy 13. A family with balanced reciprocal translocation t(8;13) in seven members and Robertsonian translocation t(13;14) in three members.
[electronic resource]
by
Gilgenkrantz, S
Defeche, C
Stehlin, S
Gregoire, M J
Producer:
19820412
In:
Human genetics
vol. 58
Online resources:
Available from publisher's website
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5.
[Union of 2 carriers of a balanced translocation. Familial study of 3 generations].
[electronic resource]
by
Gilgenkrantz, S
Grégoire, M J
Chery, M
Defèche, C
Producer:
19860305
In:
Annales de genetique
vol. 28
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6.
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis].
[electronic resource]
by
Gilgenkrantz, S
Gregoire, M J
Chery, M
Bordigoni, P
Olive, D
Producer:
19841102
In:
Journal de genetique humaine
vol. 32
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7.
Association of del(11)(p15.1p12), aniridia, catalase deficiency, and cardiomyopathy.
[electronic resource]
by
Gilgenkrantz, S
Vigneron, C
Gregoire, M J
Pernot, C
Raspiller, A
Producer:
19821216
In:
American journal of medical genetics
vol. 13
Online resources:
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8.
[Chromosome 11 and cancer].
[electronic resource]
by
Gregoire, M J
Pernot, C
Himont, F
Pierson, M
Gilgenkrantz, S
Producer:
19831123
In:
Journal de genetique humaine
vol. 31
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9.
Terminal deletion of the long arm of chromosome 10.
[electronic resource]
by
Scigliano, S
Grégoire, M J
Schmitt, M
Jonveaux, P H
LeHeup, B
Producer:
20040617
In:
Clinical genetics
vol. 65
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10.
[Phenotype of a ring-chromosome 6 carrier. Clinical and cytogenetic study].
[electronic resource]
by
Cruz-Marin, F
Gilgenkrantz, S
Gregoire, M J
Beley, G
Pierson, M
Producer:
19810528
In:
Journal de genetique humaine
vol. 28
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11.
[Translocation (3;20) and anorchism].
[electronic resource]
by
Gilgenkrantz, S
Cruz-Marin, F
Gregoire, M J
Walter, S
Pierson, M
Producer:
19820512
In:
Journal de genetique humaine
vol. 29
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12.
Refractory anaemia with excess of blasts as a terminal evolution of paroxysmal nocturnal haemoglobinuria. A case report with chromosomal analysis.
[electronic resource]
by
Aymard, J P
Buisine, J
Grégoire, M J
Janot, C
Streiff, F
Producer:
19860414
In:
Acta haematologica
vol. 74
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13.
Duplication 15q22 to 15qter and its phenotypic expression.
[electronic resource]
by
Gregoire, M J
Boue, J
Junien, C
Pernot, C
Gilgenkrantz, S
Zergollern, L
Producer:
19820527
In:
Human genetics
vol. 59
Online resources:
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14.
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) gene.
[electronic resource]
by
Bonnet, C
Grégoire, M-J
Vibert, M
Raffo, E
Leheup, B
Jonveaux, P
Producer:
20081118
In:
Journal of human genetics
vol. 53
Online resources:
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15.
Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardation.
[electronic resource]
by
Bonnet, C
Leheup, B
Béri, M
Philippe, C
Grégoire, M-J
Jonveaux, P
Producer:
20090730
In:
American journal of medical genetics. Part A
vol. 149A
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16.
Structure-photodynamic activity relationships of a series of 4-substituted zinc phthalocyanines.
[electronic resource]
by
Margaron, P
Grégoire, M J
Scasnár, V
Ali, H
van Lier, J E
Producer:
19960730
In:
Photochemistry and photobiology
vol. 63
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17.
Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterization.
[electronic resource]
by
Bonnet, C
Grégoire, M J
Brochet, K
Raffo, E
Leheup, B
Jonveaux, P
Producer:
20061108
In:
Journal of human genetics
vol. 51
Online resources:
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18.
[Microarray-based comparative genomic hybridization in the study of constitutional chromosomal abnormalities].
[electronic resource]
by
Béri-Dexheimer, M
Bonnet, C
Chambon, P
Brochet, K
Grégoire, M-J
Jonveaux, P
Producer:
20070504
In:
Pathologie-biologie
vol. 55
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19.
[Cultures of bone marrow cells in semi-solid and liquid media; value in hemopathies (apropos of 4 cases)].
[electronic resource]
by
Grégoire, M J
Umana, L
Bordigoni, P
Chiclet, A M
Gilgenkrantz, S
Streiff, F
Producer:
19831123
In:
Comptes rendus des seances de la Societe de biologie et de ses filiales
vol. 177
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20.
Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5).
[electronic resource]
by
Gilgenkrantz, S
Dulucq, P
Bresson, J L
Gouget, A
Pernot, C
Gregoire, M J
Producer:
19820521
In:
Journal of medical genetics
vol. 18
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