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Results of search for 'au:"FEINGOLD, J"', page 8 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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141.
[Incidence of cystic fibrosis in Brittany (author's transl)].
[electronic resource]
by
Demenais, F
Feingold, J
Bois, E
Jehanne, M
Toudic, L
Hennequet, A
Producer:
19800215
In:
Revue d'epidemiologie et de sante publique
vol. 27
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142.
[Chromosomal asynchrony in a case of xeroderma pigmentosum].
[electronic resource]
by
De Grouchy, J
De Nava, C
Feingold, J
Frézal, J
Lamy, M
Producer:
19680823
In:
Annales de genetique
vol. 10
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143.
[Argyria in a child following pharyngeal sprays of silver salts repeated for 6 years].
[electronic resource]
by
Marie, J
Léveque, B
Watchi, J M
Desbois, J C
Feingold, J
Producer:
19680119
In:
Annales de pediatrie
vol. 13
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144.
Genetic predisposition to West syndrome.
[electronic resource]
by
Dulac, O
Feingold, J
Plouin, P
Chiron, C
Pajot, N
Ponsot, G
Producer:
19930817
In:
Epilepsia
vol. 34
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145.
Further epidemiological evidence for anticipation in schizophrenia.
[electronic resource]
by
Gorwood, P
Leboyer, M
Falissard, B
Rouillon, F
Jay, M
Feingold, J
Producer:
19980211
In:
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
vol. 51
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146.
Ethnic difference in duration of pregnancy.
[electronic resource]
by
Papiernik, E
Cohen, H
Richard, A
de Oca, M M
Feingold, J
Producer:
19860930
In:
Annals of human biology
vol. 13
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147.
[Congenital adrenal hyperplasia (21-OH) in France. Population genetics].
[electronic resource]
by
Bois, E
Mornet, E
Chompret, A
Feingold, J
Hochez, J
Goulet, V
Producer:
19850723
In:
Archives francaises de pediatrie
vol. 42
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148.
Cystic fibrosis mutations: report from the French Registry. The Clinical Centers of the CF.
[electronic resource]
by
Guilloud-Bataille, M
De Crozes, D
Rault, G
Degioanni, A
Feingold, J
Producer:
20000620
In:
Human heredity
vol. 50
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149.
A genetic study of two French Guiana Amerindian populations. I. Serum proteins and red cell enzymes.
[electronic resource]
by
Tchen, P
Bois, E
Séger, J
Grenand, P
Feingold, N
Feingold, J
Producer:
19790425
In:
Human genetics
vol. 45
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150.
[Incidence of congenital malformations at birth in a series of maternity patients of Guadeloupe].
[electronic resource]
by
Goulet, O
Hochez, J
Berchel, C
Goulet, V
Feingold, J
Bois, E
Producer:
19870213
In:
Archives francaises de pediatrie
vol. 43
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151.
Beta-globin gene haplotypes and alpha-thalassemia analysis in Babinga pygmies from Congo-Brazzaville.
[electronic resource]
by
Mouélé, R
Bodo, J M
Mpelé, D M
Feingold, J
Galactéros, F
Producer:
20000720
In:
Human biology
vol. 72
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152.
[CALCIFICATIONS OF THE GALLBLADDER].
[electronic resource]
by
LAFITTE, A
PERIER, R
NEZELOF, C
IRIS, L
SALTIEL, H
FEINGOLD, J
Producer:
19961201
In:
Bulletins et memoires de la Societe medicale des hopitaux de Paris
vol. 115
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153.
Intellectual status of working-class children adopted early into upper-middle-class families.
[electronic resource]
by
Schiff, M
Duyme, M
Dumaret, A
Stewart, J
Tomkiewicz, S
Feingold, J
Producer:
19780814
In:
Science (New York, N.Y.)
vol. 200
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154.
Polygenic regulation of antibody synthesis to sheep erythrocytes in the mouse: a genetic analysis.
[electronic resource]
by
Feingold, N
Feingold, J
Mouton, D
Bouthillier, Y
Stiffel, C
Biozzi, G
Producer:
19761203
In:
European journal of immunology
vol. 6
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155.
Anticipation in schizophrenia: new light on a controversial problem.
[electronic resource]
by
Gorwood, P
Leboyer, M
Falissard, B
Jay, M
Rouillon, F
Feingold, J
Producer:
19961002
In:
The American journal of psychiatry
vol. 153
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156.
Vagal overactivity: a risk factor of sudden infant death syndrome?
[electronic resource]
by
Shojaei-Brosseau, T
Bonaïti-Pellie, C
Lyonnet, S
Feingold, J
Lucet, V
Producer:
20030128
In:
Archives of disease in childhood
vol. 88
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157.
[Epidemiology and genetics of ano-rectal malformations].
[electronic resource]
by
Briard, M L
Feingold, J
Kaplan, J
Bois, E
Frezal, J
Pellerin, D
Producer:
19760410
In:
Journal de genetique humaine
vol. 23 SUPPL
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158.
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo.
[electronic resource]
by
Bouanga, J C
Mouélé, R
Préhu, C
Wajcman, H
Feingold, J
Galactéros, F
Producer:
19981015
In:
Human heredity
vol. 48
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159.
[Eleven observations on a precise model of karyotype changes in the course of chronic myeloid leukemia].
[electronic resource]
by
De Grouchy, J
De Nava, C
Feingold, J
Bilski-Pasquier, G
Bousser, J
Producer:
19720320
In:
European journal of cancer
vol. 4
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160.
Homozygosity in Huntington's disease.
[electronic resource]
by
Dürr, A
Hahn-Barma, V
Brice, A
Pêcheux, C
Dodé, C
Feingold, J
Producer:
19990512
In:
Journal of medical genetics
vol. 36
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