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Results of search for 'au:"DEMINATTI, M"', page 5 of 6
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Authors
Bauters, F
Bulteel, M F
Cosson, A
Cousin, J
DEMINATTI, M
Delmas-Marsalet, Y
Deminatti, M
Deminatti, M M
Estienne, M H
Fenaux, P
Fontaine, F
Jacqueloot, N
Jouet, J P
Lai, J L
Laï, J L
MARESCAUX, J
Maillard, E
Savary, J B
Vasseur, F
Zandecki, M
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Your search returned 117 results.
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81.
[Proceedings: Familial translocation 8-12 and the multiple abnormalities syndrome].
[electronic resource]
by
Cousin, J
Savary, J B
Bayart, M
Pauli, A
Deminatti, M
Fournier, A
Producer:
19760102
In:
Pediatrie
vol. 30
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82.
[Study of a probable linkage between a genodermatosis with an autosomal dominant transmission and the MNSs blood group system].
[electronic resource]
by
Deminatti, M
Delmas-Marsalet, Y
Mennecier, M
Marquet, S
Agache, P
Huriez, C
Producer:
19690920
In:
Annales de genetique
vol. 11
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83.
[Transient leukoblastosis and dysmegakariocytopoiesis with clone 46, XX+21, t(5;7), in a newborn infant with trisomy 21].
[electronic resource]
by
Laï, J L
Zandecki, M
Weill, J
Cosson, A
Ponte, C
Deminatti, M
Producer:
19840228
In:
Nouvelle revue francaise d'hematologie
vol. 25
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84.
[Crying cat syndrome with ring shaped chromosome 5].
[electronic resource]
by
Cousin, J
Boutu, F
Savary, J B
Jacqueloot, N
Deminatti, M
Fournier, A
Producer:
19730524
In:
Archives francaises de pediatrie
vol. 29
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85.
Usefulness of linked DNA probes for prenatal diagnosis of cystic fibrosis: report of a case in a 1:4 risk pregnancy.
[electronic resource]
by
Fontaine, F
Vasseur, F
Savary, J B
Menais, M
Roussel, M
Deminatti, M M
Producer:
19880829
In:
Annales de genetique
vol. 31
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86.
Translocation (2;13)(q37;q14) in rhabdomyosarcoma: a new case.
[electronic resource]
by
Lai, J L
Savary, J B
Deminatti, M
Demaille, M C
Baranzelli, M C
Producer:
19870427
In:
Cancer genetics and cytogenetics
vol. 25
Online resources:
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87.
[Partial C trisomy through translocation t(Cp-;Gp-)].
[electronic resource]
by
Deminatti, M
Maillard, E
Gosselin, B
Peltier, J M
Bulteel, M F
Dupuis, C
Producer:
19691017
In:
Annales de genetique
vol. 12
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88.
Prenatal diagnosis of PIBIDS.
[electronic resource]
by
Savary, J B
Vasseur, F
Vinatier, D
Manouvrier, S
Thomas, P
Deminatti, M M
Producer:
19920130
In:
Prenatal diagnosis
vol. 11
Online resources:
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89.
A new case of dic(9;12)(p13;p11) in acute lymphocytic leukemia.
[electronic resource]
by
Lai, J L
Deminatti, M
Estienne, M H
Zandecki, M
Nelken, B
Fenaux, P
Producer:
19891121
In:
Cancer genetics and cytogenetics
vol. 42
Online resources:
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90.
[Ichthyosis linked to the X chromosome. Biochemical and endocrinologic study].
[electronic resource]
by
Weill, J
Vasseur, F
Savary, J B
Stuckens, C
Deminatti, M M
Ponte, C
Producer:
19891219
In:
Pediatrie
vol. 44
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91.
[Chromosomal study of human hermaphroditism. Apropos of a case with 46,XY 46,-XX karyotpe].
[electronic resource]
by
Saint-Aubert, P
Maillard, E
Walbaum, R
Delmas-Marsalet, Y
Deminatti, M
Fontaine, G
Producer:
19680523
In:
Annales de pediatrie
vol. 15
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92.
Cytogenetic studies in 30 patients with Burkitt's lymphoma or L3 acute lymphoblastic leukemia with special reference to additional chromosome abnormalities.
[electronic resource]
by
Lai, J L
Fenaux, P
Zandecki, M
Nelken, B
Huart, J J
Deminatti, M
Producer:
19890814
In:
Annales de genetique
vol. 32
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93.
Is translocation (8;21) a "favorable" cytogenetic rearrangement in acute myeloid leukemia?
[electronic resource]
by
Fenaux, P
Laï, J L
Preudhomme, C
Jouet, J P
Deminatti, M
Bauters, F
Producer:
19901114
In:
Nouvelle revue francaise d'hematologie
vol. 32
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94.
[Subacute pre-eclampsia and hydramnios as manifestation of fetal triploidy. In utero diagnosis in the 28th week].
[electronic resource]
by
Dognin, C
Monnier, J C
Lanciaux, B
Savary, J B
Deminatti, M
Gosselin, B
Producer:
19840224
In:
Journal de gynecologie, obstetrique et biologie de la reproduction
vol. 12
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95.
[The cardiopathies of Ullrich-Turner syndrome].
[electronic resource]
by
Dupuis, C
Deminatti, M
Maillard, E
Nuyts, J P
Cousin, J
Frison, B
Walbaum, R
Producer:
19710803
In:
Archives francaises de pediatrie
vol. 28
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96.
Chronic myelogenous leukemia with t(9;22) and t(8;11): a new chromosome anomaly.
[electronic resource]
by
Laï, J L
Jouet, J P
Savary, J B
Fenaux, P
Bauters, F
Deminatti, M
Producer:
19870318
In:
Cancer genetics and cytogenetics
vol. 25
Online resources:
Available from publisher's website
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97.
[Burkitt's acute lymphoblastic leukemia. Incidence and cytogenetic aspects].
[electronic resource]
by
Laï, J L
Jouet, J P
Zandecki, M
Huart, J J
Bauters, F
Deminatti, M
Producer:
19840224
In:
Nouvelle revue francaise d'hematologie
vol. 25
Availability:
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98.
Cytogenetics and their prognostic value in childhood and adult acute lymphoblastic leukemia (ALL) excluding L3.
[electronic resource]
by
Fenaux, P
Lai, J L
Morel, P
Nelken, B
Taboureau, O
Deminatti, M
Bauters, F
Producer:
19890808
In:
Hematological oncology
vol. 7
Online resources:
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99.
Translocations (5;17) and (7;17) in patients with de novo or therapy-related myelodysplastic syndromes or acute nonlymphocytic leukemia. A possible association with acquired pseudo-Pelger-Huët anomaly and small vacuolated granulocytes.
[electronic resource]
by
Laï, J L
Zandecki, M
Fenaux, P
Le Baron, F
Bauters, F
Cosson, A
Deminatti, M
Producer:
19900626
In:
Cancer genetics and cytogenetics
vol. 46
Online resources:
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100.
[Men with karyotype 46, XX (apropos of 2 cases)].
[electronic resource]
by
Fossati, P
Savary, J B
Boutemy, J J
Dewailly, D
François, M
Lai, J L
Deminatti, M
Producer:
19800425
In:
Lille medical : journal de la Faculte de medecine et de pharmacie de l'Universite de Lille
vol. 24
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