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Results of search for 'au:"FEINGOLD, J"', page 10 of 16
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Authors
Bilgrami, S
Bois, E
Bona, R D
Briard, M L
Brice, A
Demenais, F
Dorsky, D
Dürr, A
Edwards, R L
Emerit, I
Feingold, J
Feingold, J M
Feingold, N
Frezal, J
Frézal, J
Gorwood, P
Guilloud-Bataille, M
Kauffmann, F
Leboyer, M
Tutschka, P J
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181.
HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.
[electronic resource]
by
Couillin, P
Rappaport, R
Kuttenn, F
Hors, J
Feingold, J
Boué, J
Boué, A
Producer:
19860311
In:
Annals of the New York Academy of Sciences
vol. 458
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182.
Genetic heterogeneity of Alport syndrome.
[electronic resource]
by
Feingold, J
Bois, E
Chompret, A
Broyer, M
Gubler, M C
Grünfeld, J P
Producer:
19850822
In:
Kidney international
vol. 27
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183.
Risk factors of malaria infection during pregnancy in Burkina Faso: suggestion of a genetic influence.
[electronic resource]
by
Cot, M
Abel, L
Roisin, A
Barro, D
Yada, A
Carnevale, P
Feingold, J
Producer:
19930510
In:
The American journal of tropical medicine and hygiene
vol. 48
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184.
Genetic predisposition to severe myoclonic epilepsy in infancy.
[electronic resource]
by
Benlounis, A
Nabbout, R
Feingold, J
Parmeggiani, A
Guerrini, R
Kaminska, A
Dulac, O
Producer:
20010329
In:
Epilepsia
vol. 42
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185.
Revisiting metatropic dysplasia: presentation of a series of 19 novel patients and review of the literature.
[electronic resource]
by
Geneviève, D
Le Merrer, M
Feingold, J
Munnich, A
Maroteaux, P
Cormier-Daire, V
Producer:
20080429
In:
American journal of medical genetics. Part A
vol. 146A
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186.
[Frequency of birth defects. Study of a maternity hospital in Paris].
[electronic resource]
by
Briard, M L
Feingold, J
Bonaiti-Pellie, C
Lapeyre, F
Frezal, J
Varangot, J
Producer:
19760429
In:
Archives francaises de pediatrie
vol. 32
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187.
Genetic control of macrophage functions. I. Polygenic regulation of phagocytosis stimulation produced by Glyceryl Trioleate.
[electronic resource]
by
Mouton, D
Bouthillier, Y
Feingold, N
Feingold, J
Decreusefond, C
Stiffel, C
Biozzi, G
Producer:
19750517
In:
The Journal of experimental medicine
vol. 141
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188.
[Confirmation of the localization of the locus of phosphoglyceratekinase on the X chromosome by the method of human-mouse cellular hybridization].
[electronic resource]
by
Picard, J Y
Billardon, C
Le Borgne de Kaouel, C
Feingold, J
Frézal, J
Producer:
19710930
In:
Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles
vol. 273
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189.
HLA, Pi, Gm and Km phenotypes in a spina bifida population with myelo-meningocele.
[electronic resource]
by
Vannier, J P
Cavelier, B
Martin, J P
Lefort, J
Rivat, L
Feingold, J
Producer:
19810226
In:
Tissue antigens
vol. 15
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190.
Studies on an isolated West Indies population. III. Epidemiologic study of sensorineural hearing loss.
[electronic resource]
by
Bois, E
Bonaïti, C
Lallemant, M
Moatti, L
Feingold, N
Mayer, F M
Feingold, J
Producer:
19871103
In:
Neuroepidemiology
vol. 6
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191.
[Congenital cataract linked to the Y chromosome].
[electronic resource]
by
Feingold, J
Raoul, O
See, G
Delthil, S
Crouzet, J
Demailly, M L
Morel, J
Producer:
19791128
In:
Journal de genetique humaine
vol. 27
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192.
Genetic control of blood infection levels in human malaria: evidence for a complex genetic model.
[electronic resource]
by
Garcia, A
Cot, M
Chippaux, J P
Ranque, S
Feingold, J
Demenais, F
Abel, L
Producer:
19980507
In:
The American journal of tropical medicine and hygiene
vol. 58
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193.
[Parent's information and prenatal diagnosis of cerebral malformation with an uncertain prognosis].
[electronic resource]
by
Moutard, M-L
Fauriel, I
Moutel, G
François, I
Feingold, J
Ponsot, G
Hervé, C
Producer:
20040720
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 11
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194.
Mode of inheritance in familial cases of primary gonadotropic deficiency.
[electronic resource]
by
Chaussain, J L
Toublanc, J E
Feingold, J
Naud, C
Vassal, J
Job, J C
Producer:
19890321
In:
Hormone research
vol. 29
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195.
[Ethnic variation of the duration of gestation].
[electronic resource]
by
Papiernik, E
Montès de Oca, M
de Mouzon, J
Hilbert, J
Cohen, H
Feingold, J
Producer:
19860207
In:
Archives francaises de pediatrie
vol. 42 Suppl 1
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196.
Chromosome 11q localization of one of the three expected genes for the human alpha-3-fucosyltransferases, by somatic hybridization.
[electronic resource]
by
Couillin, P
Mollicone, R
Grisard, M C
Gibaud, A
Ravisé, N
Feingold, J
Oriol, R
Producer:
19910514
In:
Cytogenetics and cell genetics
vol. 56
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197.
Inheritance of abnormal erythrocyte cation transport in essential hypertension.
[electronic resource]
by
Meyer, P
Garay, R P
Nazaret, C
Dagher, G
Bellet, M
Broyer, M
Feingold, J
Producer:
19810810
In:
British medical journal (Clinical research ed.)
vol. 282
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198.
[Prevalence of etinoblastoma in the Midi-Pyrenées area].
[electronic resource]
by
Bonaiti-Pellie, C
Colombies, P
Bec, P
Briard-Guillemot, M L
Feingold, J
Frezal, J
Producer:
19760602
In:
Annales de genetique
vol. 18
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199.
[Incidence of pancreatic cystic fibrosis in France].
[electronic resource]
by
Feingold, J
Hennequet, A
Jehanne, M
Feigelson, J
Toudic, L
Quiniou, O
Briard, M L
Producer:
19750505
In:
Annales de genetique
vol. 17
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200.
[Plasmodium falciparum malaria and sickle cell gene in the popular Republic of Congo. I. Relationship between parasitemia and sicke cell trait in Djoumouna (region of Brazzaville) (author's transl)].
[electronic resource]
by
Carnevale, P
Bosseno, M F
Lallemant, M
Feingold, J
Lissouba, P
Molinier, M
Mouchet, J
Producer:
19820420
In:
Annales de genetique
vol. 24
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