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Results of search for 'au:"Chéry, M"', page 1 of 2
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Authors
Abbadi, N
Abbas, N
André, M
Arnould, C
Bach, I
Benit, P
Biancalana, V
Bienvenu, T
Bieth, E
Chery, M
Chéry, M
Cremers, F P
Fardeau, M
Gilgenkrantz, S
Gregoire, M J
Hanauer, A
Jonveaux, P
Mandel, J L
Mujica, P
Philippe, C
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Topics
Adult
Animals
Blotting, Southern
Child
Child, Preschool
Chromosome Banding
Chromosome Mapping
DNA Probes
Female
Genetic Linkage
Genetic Markers
Humans
Karyotyping
Male
Pedigree
Sex Chromosome Aberrations
Translocation, Genetic
X Chromosome
abnormalities
genetics
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English
French
Your search returned 30 results.
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1.
Crossing boundaries to improve mental health in the Americas: international collaborative authorship.
[electronic resource]
by
Killion, Chery M
Producer:
20071016
In:
The ABNF journal : official journal of the Association of Black Nursing Faculty in Higher Education, Inc
vol. 18
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2.
Chromosome rearrangements and human gene mapping.
[electronic resource]
by
Gilgenkrantz, S
Philippe, C
Chery, M
Producer:
19950126
In:
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
vol. 48
Online resources:
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3.
Potential use of BacT/Alert automated blood culture system for antifungal susceptibility testing.
[electronic resource]
by
Hazen, K C
Chery, M P
Han, Y
Producer:
19940630
In:
Journal of clinical microbiology
vol. 32
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4.
The Noonan syndrome. The Nancy experience revisited.
[electronic resource]
by
Chery, M
Philippe, C
Worms, A M
Gilgenkrantz, S
Producer:
19930928
In:
Genetic counseling (Geneva, Switzerland)
vol. 4
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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.
[Balanced X-autosomal translocation and mental retardation. Mapping mental retardation linked to X (excluding fragile X)].
[electronic resource]
by
Teboul, M
Mujica, P
Chery, M
Leotard, B
Gilgenkrantz, S
Producer:
19900410
In:
Journal de genetique humaine
vol. 37
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7.
[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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8.
X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe.
[electronic resource]
by
Camus, P
Abbadi, N
Perrier, M C
Chéry, M
Gilgenkrantz, S
Producer:
19960307
In:
Human genetics
vol. 97
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9.
Use of Gen-Probe and Bactec for rapid isolation and identification of mycobacteria. Correlation of probe results with growth index.
[electronic resource]
by
Body, B A
Warren, N G
Spicer, A
Henderson, D
Chery, M
Producer:
19900402
In:
American journal of clinical pathology
vol. 93
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10.
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.
[electronic resource]
by
Hanauer, A
Chery, M
Fujita, R
Driesel, A J
Gilgenkrantz, S
Mandel, J L
Producer:
19900206
In:
American journal of human genetics
vol. 46
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11.
Interstitial deletion of the long arm of chromosome 6.
[electronic resource]
by
Chery, M
Formiga, L F
Mujica, P
André, M
Stehelin, D
Dozier, C
Gilgenkrantz, S
Producer:
19890901
In:
Annales de genetique
vol. 32
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12.
Physical mapping of DNA markers in the q13-q22 region of the human X chromosome.
[electronic resource]
by
Philippe, C
Cremers, F P
Chery, M
Bach, I
Abbadi, N
Ropers, H H
Gilgenkrantz, S
Producer:
19931022
In:
Genomics
vol. 17
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13.
Mosaic tetrasomy 12p.
[electronic resource]
by
Gilgenkrantz, S
Droulle, P
Schweitzer, M
Foliguet, B
Chadefaux, B
Lombard, M
Chery, M
Prieur, M
Producer:
19860219
In:
Clinical genetics
vol. 28
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14.
De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemia.
[electronic resource]
by
Martel, V
Guerci, A
Humbert, J C
Gregoire, M J
Chery, M
Lederlin, P
Jonveaux, P
Producer:
19971223
In:
British journal of haematology
vol. 99
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15.
[Familial supravalvular aortic stenosis. Investigation in a family and review of the literature].
[electronic resource]
by
Burnel, P
Marçon, F
Lucron, H
Bosser, G
Gilgenkrantz, S
Jonveaux, P
Chéry, M
Worms, A M
Producer:
19970925
In:
Archives des maladies du coeur et des vaisseaux
vol. 90
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16.
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.
[electronic resource]
by
Chery, M
Biancalana, V
Philippe, C
Malpuech, G
Carla, H
Gilgenkrantz, S
Mandel, J L
Hanauer, A
Producer:
19940602
In:
Human genetics
vol. 93
Online resources:
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17.
Monosomy 21q: two cases of del(21q) and review of the literature.
[electronic resource]
by
Huret, J L
Léonard, C
Chery, M
Philippe, C
Schafei-Benaissa, E
Lefaure, G
Labrune, B
Gilgenkrantz, S
Producer:
19960228
In:
Clinical genetics
vol. 48
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18.
Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markers.
[electronic resource]
by
Serville, F
Benit, P
Saugier, P
Vibert, M
Royer, G
Pelet, A
Chery, M
Munnich, A
Lyonnet, S
Producer:
19931014
In:
Prenatal diagnosis
vol. 13
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19.
Chromosomal mapping of the human (MACS) and mouse (Macs) genes encoding the MARCKS protein.
[electronic resource]
by
Blackshear, P J
Tuttle, J S
Oakey, R J
Seldin, M F
Chery, M
Philippe, C
Stumpo, D J
Producer:
19921222
In:
Genomics
vol. 14
Online resources:
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20.
Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas.
[electronic resource]
by
Gilgenkrantz, S
Chery, M
Teboul, M
Mujica, P
Leotard, B
Gregoire, M J
Boman, F
Duprez, A
Hanauer, A
Producer:
19900830
In:
Oncogene
vol. 5
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