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Results of search for 'au:"Vámos, E"', page 4 of 7
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Authors
Andrien, M
Avni, F
Blum, D
Cochaux, P
Courtens, W
Dodion, J
Donner, C
Dupont, E
Elkhazen, N
Elmer, C
Ferster, A
Flament-Durand, J
Heimann, P
Jauniaux, E
Liebaers, I
Lissens, W
Rodesch, F
Vamos, E
Van Regemorter, N
Vámos, E
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Topics
Abnormalities, Multiple
Adult
Cells, Cultured
Child, Preschool
Chromosome Aberrations
Female
Humans
Infant
Infant, Newborn
Karyotyping
Male
Pregnancy
Prenatal Diagnosis
Syndrome
abnormalities
analysis
blood
diagnosis
genetics
metabolism
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Your search returned 122 results.
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61.
[Chorionic villi sampling: experience of the initial 500 samples].
[electronic resource]
by
Donner, C
Simon, P
Gosselin, F
Vamos, E
Cochaux, P
Vassart, G
Rodesch, F
Producer:
19900823
In:
Revue medicale de Bruxelles
vol. 11
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62.
Value of glial fibrillary acidic protein determination in amniotic fluid for prenatal diagnosis of neural tube defects.
[electronic resource]
by
Van Regemorter, N
Gheuens, J
Noppe, M
Vamos, E
Seller, M J
Lowenthal, A
Producer:
19870828
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 165
Online resources:
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63.
Infantile form of sialic acid storage disorder: clinical, ultrastructural, and biochemical studies in two siblings.
[electronic resource]
by
Tondeur, M
Libert, J
Vamos, E
Van Hoof, F
Thomas, G H
Strecker, G
Producer:
19830311
In:
European journal of pediatrics
vol. 139
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64.
Vasopressin and gonadotropin deficiency in a boy with the ectrodactyly-ectodermal dysplasia-clefting syndrome.
[electronic resource]
by
Van Maldergem, L
Gillerot, Y
Vamos, E
Toppet, M
Watillon, P
Van Vliet, G
Producer:
19920723
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 81
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65.
[Echographic evaluation of non-immunologic feto-placental anasarca. A series of 24 cases].
[electronic resource]
by
Elkhazen, N
Jauniaux, E
Dodion, J
Vamos, E
Rodesch, F
Wilkin, P
Milaire, J
Producer:
19860611
In:
Journal de gynecologie, obstetrique et biologie de la reproduction
vol. 15
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66.
A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis.
[electronic resource]
by
Seneca, S
Abramowicz, M
Lissens, W
Muller, M F
Vamos, E
de Meirleir, L
Producer:
19961004
In:
Journal of inherited metabolic disease
vol. 19
Online resources:
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67.
Cutaneous porphyria in a neonate with tyrosinaemia type 1.
[electronic resource]
by
Vanden Eijnden, S
Blum, D
Clercx, A
Goyens, P
De Laet, C
Vamos, E
Producer:
20010108
In:
European journal of pediatrics
vol. 159
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68.
Influence of recombinant gamma-interferon on enhancement of major histocompatibility complex class II antigen expression and functional immunological capacities of human amniotic and chorionic villi cells.
[electronic resource]
by
Gotlieb, W
Wybran, J
Romasco, F
Vamos, E
Andrien, M
Rodesch, F
Dupont, E
Producer:
19870330
In:
Transplantation proceedings
vol. 19
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69.
Prenatal diagnosis and fetal pathology of partial trisomy 20P-monosomy 4P resulting from paternal translocation.
[electronic resource]
by
Vamos, E
Pratola, D
Van Regemorter, N
Freund, M
Flament-Durand, J
Rodesch, F
Producer:
19850827
In:
Prenatal diagnosis
vol. 5
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70.
Alterations in cultured fibroblasts of sibs with an infantile form of a free (unbound) sialic acid storage disorder.
[electronic resource]
by
Thomas, G H
Scocca, J
Libert, J
Vamos, E
Miller, C S
Reynolds, L W
Producer:
19830715
In:
Pediatric research
vol. 17
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71.
[Collection of fetal cord blood for karyotyping].
[electronic resource]
by
Donner, C
Avni, F
Karoubi, R
Simon, P
Vamos, E
Van Regemorter, N
Rodesch, F
Producer:
19920612
In:
Journal de gynecologie, obstetrique et biologie de la reproduction
vol. 21
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72.
[Cold hemagglutinin disease revealing an intramucosal carcinoma of the stomach (author's transl)].
[electronic resource]
by
Lustman, F
Salhadin, A
Andre, P
Vamos, E
Csoma, M
Dupont, J M
Jamsin, S
Producer:
19790927
In:
Acta gastro-enterologica Belgica
vol. 42
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73.
Cholesteryl ester storage disease with secondary lecithin cholesterol acyl transferase deficiency.
[electronic resource]
by
Van Erum, S
Gnat, D
Finne, C
Blum, D
Vanhelleput, C
Vamos, E
Vertongen, F
Producer:
19881215
In:
Journal of inherited metabolic disease
vol. 11 Suppl 2
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74.
[Leukemia lymphoma T-cell as first manifestation of ataxia-telangiectasia].
[electronic resource]
by
de Laet, C
Casimir, G
Duchâteau, J
Vamos, E
Devalck, C
Sariban, E
Ferster, A
Producer:
19961211
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 3
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75.
[The value of prenatal chromosomal diagnosis in cases of fetal abnormalities: results obtained in 468 pathological pregnancies].
[electronic resource]
by
Vamos, E
Elmer, C
Lévi, S
el Khazen, N
Donner, C
Avni, F
Rodesch, F
Producer:
19900823
In:
Revue medicale de Bruxelles
vol. 11
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76.
Differential inducibility of HLA class I and II antigens by r-IFN gamma in type III bare lymphocyte syndrome.
[electronic resource]
by
Andrien, M
Stordeur, P
Vamos, E
Mascart Lemone, F
Toungouz, M
Monfils, G
Dupont, E
Producer:
19910305
In:
Transplantation proceedings
vol. 23
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77.
[Prenatal diagnosis of digestive system malformations using echography].
[electronic resource]
by
Elkhazen, N
Dodion, J
Vamos, E
Van Regemorter, N
Perlmutter, N
Flici, O
Rodesch, F
Producer:
19850124
In:
Revue medicale de Bruxelles
vol. 5
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78.
Partial trisomy 3p in two siblings: clinical and pathological findings.
[electronic resource]
by
Van Regemorter, N
Vamos, E
Gillerot, Y
Viteux, V
Hayez, F
Pardou, A
Flament-Durand, J
Producer:
19840127
In:
European journal of pediatrics
vol. 141
Online resources:
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79.
Deletion of chromosome 11p13-11p15.5 sequences in invasive human ovarian cancer is a subclonal progression factor.
[electronic resource]
by
Vandamme, B
Lissens, W
Amfo, K
De Sutter, P
Bourgain, C
Vamos, E
De Grève, J
Producer:
19921216
In:
Cancer research
vol. 52
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80.
[Nanism with short limbs, dysmorphism, renal dysplasia, growth hormone deficiency with pituitary hypoplasia and psychomotor delay: a new syndrome?].
[electronic resource]
by
Elmer, C
Van Vliet, G
Heinrichs, C
Toppet, M
Christophe, C
Perlmutter-Cremer, N
Vamos, E
Producer:
19900618
In:
Journal de genetique humaine
vol. 37
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