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Results of search for 'au:"BOUE, A"', page 11 of 15
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BOUE, A
Boue, A
Boue, J
Boué, A
Boué, J
Boué, J G
CELERS, J
Cabau, N
Celers, J
Couillin, P
Deluchat, C
Junien, C
Mathieu-Boué, A
Mornet, E
Muller, F
Nicolas, H
Oury, J F
Serre, J L
Simon-Bouy, B
Taillandier, A
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Topics
Abortion, Spontaneous
Adult
Amniotic Fluid
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Female
France
Humans
Infant, Newborn
Karyotyping
Male
Pregnancy
Prenatal Diagnosis
Trisomy
analysis
diagnosis
genetics
immunology
methods
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English
French
Undetermined
Your search returned 292 results.
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201.
[Identification by Q and G bands of chromosome anomalies in spontaneous abortion].
[electronic resource]
by
Boué, J
Daketsé, M J
Deluchat, C
Ravisé, N
Yvert, F
Boué, A
Producer:
19770331
In:
Annales de genetique
vol. 19
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202.
Androgenetic origin of African complete hydatidiform moles demonstrated by HLA markers.
[electronic resource]
by
Couillin, P
Afoutou, J M
Faye, O
Ravisé, N
Correa, P
Boué, A
Producer:
19851118
In:
Human genetics
vol. 71
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203.
Chromosomal localization of human genes governing the interferon-induced antiviral state.
[electronic resource]
by
Chany, C
Vignal, M
Couillin, P
Van Cong, N
Boué, J
Boué, A
Producer:
19760116
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 72
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204.
[Requests for prenatal diagnosis from parents of children with cystic fibrosis].
[electronic resource]
by
Demay, G
Stubnicer, A C
Boué, A
Boué, J
Pechevis, M
Lenoir, G
Producer:
19861118
In:
Journal de genetique humaine
vol. 34
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205.
Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndrome.
[electronic resource]
by
Tejada, M I
Mornet, E
Tizzano, E
Molina, M
Baiget, M
Boue, A
Producer:
19940510
In:
Journal of medical genetics
vol. 31
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206.
Evidence for synteny between a polio receptor gene and glucose phosphate isomerase (GPI) by analysis of human-mouse hybrids.
[electronic resource]
by
Couillin, P
Boué, A
Van Cong, N
Weil, D
Rebourcet, R
Frézal, J
Producer:
19761223
In:
Cytogenetics and cell genetics
vol. 16
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207.
[A prospective study of Cytomegalovirus infections in 211 children with renal transplants].
[electronic resource]
by
Cabau, N
Gagnadoux, M F
Niaudet, P
Duros, C
Broyer, M
Boué, A
Producer:
19830920
In:
Annales de pediatrie
vol. 30
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208.
Prenatal diagnosis of cystic fibrosis: ultrasonography of the gallbladder at 17-19 weeks of gestation.
[electronic resource]
by
Duchatel, F
Muller, F
Oury, J F
Mennesson, B
Boue, J
Boue, A
Producer:
19930419
In:
Fetal diagnosis and therapy
vol. 8
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209.
Health of long term benzodiazepine users.
[electronic resource]
by
Halfon, P
Le Bras, P
Le Goc, I
Mathieu-Boue, A
Feline, A
Producer:
19880718
In:
British medical journal (Clinical research ed.)
vol. 296
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210.
[Prospective study of cytomegalovirus infections in 211 children with kidney transplants].
[electronic resource]
by
Cabau, N
Gagnadoux, M F
Niaudet, P
Duros, C
Broyer, M
Boue, A
Producer:
19840319
In:
La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris
vol. 59
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211.
Quality of the humoral immunity conferred by RA 27-3 rubella vaccine.
[electronic resource]
by
Montagnon, B
Boué, A
Nicolas, A
Tayot, J L
Peyron, L
Servajean, B
Producer:
19740827
In:
Biomedicine / [publiee pour l'A.A.I.C.I.G.]
vol. 19
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212.
[Seroepidemiology of herpesvirus hominis and cytomegalovirus infections in the first 4 years of life (author's transl)].
[electronic resource]
by
Cabau, N
Coignard, S
Labadie, M D
Coulon, M
Duros, C
Boué, A
Producer:
19810219
In:
Archives francaises de pediatrie
vol. 37 Suppl 2
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213.
[Sero-epidemiology of infections due to cytomegalovirus by indirect hemagglutination technic].
[electronic resource]
by
Boue, A
Perraudin, N
Celers, J
Dreyfus, J
Schneegans, P
Gueguen, S
Lazar, P
Producer:
19761002
In:
Archives francaises de pediatrie
vol. 33
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214.
Genetic differences between cystic fibrosis with and without meconium ileus.
[electronic resource]
by
Simon-Bouy, B
Serre, J L
Mornet, E
Tallandier, A
Boué, J
Boué, A
Producer:
19890810
In:
Lancet (London, England)
vol. 2
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215.
Affected sibs with fragile X syndrome exhibit an age-dependent decrease in the size of the fragile X full mutation.
[electronic resource]
by
Mornet, E
Jokic, M
Bogyo, A
Tejada, I
Deluchat, C
Boué, J
Boué, A
Producer:
19930701
In:
Clinical genetics
vol. 43
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216.
Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients.
[electronic resource]
by
Simon-Bouy, B
Mornet, E
Serre, J L
Taillandier, A
Boué, J
Boué, A
Producer:
19920305
In:
Clinical genetics
vol. 40
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217.
[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].
[electronic resource]
by
Mornet, E
Boué, J
Crète, P
Raux-Demay, M C
Kutten, F
Boué, A
Producer:
19920423
In:
Archives francaises de pediatrie
vol. 49
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218.
[Confirmation of the localization on human chromosome F19 of a structural gene of poliovirus receptors].
[electronic resource]
by
Couillin, M M
Boué, A
Van-Cong, N
Weil, D
Rebourcet, R
Frézal, J
Producer:
19760221
In:
Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles
vol. 281
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219.
[HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population].
[electronic resource]
by
Couillin, P
Ravisé, N
Hors, J
Feingold, J
Rappaport, R
Kuttenn, F
Boué, A
Producer:
19861118
In:
Pathologie-biologie
vol. 34
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220.
Demonstration of human kidney differentiation antigens with monoclonal antibodies.
[electronic resource]
by
Candelier, J J
Couillin, P
Bellon, G
Le Pendu, J
Eydoux, P
Boue, A
Producer:
19881024
In:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
vol. 36
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