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Results of search for 'au:"FEINGOLD, J"', page 2 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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21.
Senior Eye Gallery a sight to behold.
[electronic resource]
by
Feingold, J F
Producer:
19870911
In:
Provider (Washington, D.C.)
vol. 13
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22.
Genetics of Alport's syndrome.
[electronic resource]
by
Feingold, J
Bois, E
Producer:
19901227
In:
Pediatric nephrology (Berlin, Germany)
vol. 1
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23.
[Genetics of blood uric acid levels: study of 3 Amerindian tribes of Upper French Guyana].
[electronic resource]
by
Bois, E
Feingold, J
Producer:
19730305
In:
Annales de genetique
vol. 15
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24.
[Presymptomatic diagnosis in genetics: the model of Huntington disease].
[electronic resource]
by
Feingold, J
Dürr, A
Producer:
19971002
In:
Pathologie-biologie
vol. 45
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25.
Do parents and grandparents of patients with achondroplasia have a higher cancer risk?
[electronic resource]
by
Stoll, C
Feingold, J
Producer:
20050208
In:
American journal of medical genetics. Part A
vol. 130A
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26.
Idiopathic haemochromatosis: an autosomal recessive disease.
[electronic resource]
by
Saddi, R
Feingold, J
Producer:
19740828
In:
Clinical genetics
vol. 5
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27.
[Idiopathic hemochromatosis and diabetes].
[electronic resource]
by
Saddi, R
Feingold, J
Producer:
19690808
In:
Revue francaise d'etudes cliniques et biologiques
vol. 14
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28.
Estimating prevalence in single-gene kidney diseases progressing to renal failure.
[electronic resource]
by
Levy, M
Feingold, J
Producer:
20001012
In:
Kidney international
vol. 58
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29.
[Idiopathic hemochromatosis. Autosomal recessive disease].
[electronic resource]
by
Saddi, R
Feingold, J
Producer:
19690808
In:
Revue francaise d'etudes cliniques et biologiques
vol. 14
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30.
Idiopathic haemochromatosis and diabetes mellitus.
[electronic resource]
by
Saddi, R
Feingold, J
Producer:
19740828
In:
Clinical genetics
vol. 5
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31.
[Genetics of the Alport syndrome. Hereditary nephropathy with deafness].
[electronic resource]
by
Feingold, J
Bois, E
Producer:
19710903
In:
Humangenetik
vol. 12
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32.
Genetic comparisons of patients with cystic fibrosis with or without meconium ileus. Clinical Centers of the French CF Registry.
[electronic resource]
by
Feingold, J
Guilloud-Bataille, M
Producer:
19991118
In:
Annales de genetique
vol. 42
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33.
An autonomously replicating eukaryotic expression vector with a tetracycline-responsive promoter.
[electronic resource]
by
Lang, Z
Feingold, J M
Producer:
19960726
In:
Gene
vol. 168
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34.
[Parental age in embryonic neoplasms].
[electronic resource]
by
Bonaiti-Pellie, C
Feingold, J
Producer:
19800514
In:
Revue d'epidemiologie et de sante publique
vol. 27
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35.
[Parental age in embryonic neoplasms].
[electronic resource]
by
Bonaiti-Pellie, C
Feingold, J
Producer:
19800514
In:
Revue d'epidemiologie et de sante publique
vol. 27
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36.
[Conditions and limitations of healthy carrier screening for the mutation responsible for cystic fibrosis].
[electronic resource]
by
Serre, J L
Feingold, J
Producer:
19940217
In:
Revue d'epidemiologie et de sante publique
vol. 41
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37.
[Parental age and mutation. Apropos of a study of Duchenne de Boulogne's myopathy].
[electronic resource]
by
Pellié, C
Feingold, J
Demos, J
Producer:
19731211
In:
Journal de genetique humaine
vol. 21
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38.
[Major genes, modifying genes, and environmental effect of Duchenne de Boulogne myopathy].
[electronic resource]
by
Feingold, J
Feingold, N
Demos, J
Producer:
19711215
In:
Annales de genetique
vol. 14
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39.
Chromosomal breakage and scleroderma: studies in family members.
[electronic resource]
by
Emerit, I
Housset, E
Feingold, J
Producer:
19760823
In:
The Journal of laboratory and clinical medicine
vol. 88
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40.
[Chromosome effect of cyclophosphamide in various strains of mice].
[electronic resource]
by
Emerit, I
Levy, A
Feingold, J
Producer:
19761230
In:
Annales de genetique
vol. 19
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