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	21.	Increased expression of the c-fos proto-oncogene in bone from patients with fibrous dysplasia. [electronic resource] by Candeliere, G A Glorieux, F H Prud'homme, J St-Arnaud, R Producer: 19950608 In: The New England journal of medicine vol. 332 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Intrathoracic tumor with hypoglycemia. [electronic resource] by Pontius, J R Seidel, J Reveley, H Prud'homme, J Heaney, J P Producer: 19671117 In: Texas medicine vol. 63 Availability: No items available. Save to lists Add to cart (remove)
	23.	CGI-58/ABHD5 gene is mutated in Dorfman-Chanarin syndrome. [electronic resource] by Caux, F Selma, Z Ben Laroche, L Prud'homme, J F Fischer, J Producer: 20050318 In: American journal of medical genetics. Part A vol. 129A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Targeted inactivation of the 25-hydroxyvitamin D(3)-1(alpha)-hydroxylase gene (CYP27B1) creates an animal model of pseudovitamin D-deficiency rickets. [electronic resource] by Dardenne, O Prud'homme, J Arabian, A Glorieux, F H St-Arnaud, R Producer: 20010719 In: Endocrinology vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Genetic linkage of Meleda disease to chromosome 8qter. [electronic resource] by Fischer, J Bouadjar, B Heilig, R Fizames, C Prud'homme, J F Weissenbach, J Producer: 19990312 In: European journal of human genetics : EJHG vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Correction of the abnormal mineral ion homeostasis with a high-calcium, high-phosphorus, high-lactose diet rescues the PDDR phenotype of mice deficient for the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1). [electronic resource] by Dardenne, O Prud'homme, J Hacking, S A Glorieux, F H St-Arnaud, R Producer: 20031211 In: Bone vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Monoclonal antibodies against native ant denatured forms of estrogen-induced breast cancer protein (BCEI/pS2) obtained by expression in Escherichia coli. [electronic resource] by Prud'homme, J F Jolivet, A Pichon, M F Savouret, J F Milgrom, E Producer: 19900503 In: Cancer research vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	28.	Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity. [electronic resource] by Parmentier, L Blanchet-Bardon, C Nguyen, S Prud'homme, J F Dubertret, L Weissenbach, J Producer: 19951215 In: Human molecular genetics vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Immunohistochemistry of pS2 in normal human breast and in various histological forms of breast tumours. [electronic resource] by Pallud, C Le Doussal, V Pichon, M F Prud'homme, J F Hacene, K Milgrom, E Producer: 19931209 In: Histopathology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	[Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis]. [electronic resource] by von Fellenberg, J Paternotte, C Prud'homme, J F Weissenbach, J Hazan, J Burgunder, J M Producer: 19980901 In: Schweizerische medizinische Wochenschrift vol. 128 Availability: No items available. Save to lists Add to cart (remove)
	31.	Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families. [electronic resource] by Gücüyener, K Ozgül, K Paternotte, C Erdem, H Prud'homme, J F Ozgüç, M Topaloğlu, H Producer: 20011011 In: Neuropediatrics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	HES6 acts as a transcriptional repressor in myoblasts and can induce the myogenic differentiation program. [electronic resource] by Gao, X Chandra, T Gratton, M O Quélo, I Prud'homme, J Stifani, S St-Arnaud, R Producer: 20011025 In: The Journal of cell biology vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region. [electronic resource] by Fischer, J Blanchet-Bardon, C Prud'homme, J F Pavek, S Steijlen, P M Dubertret, L Weissenbach, J Producer: 19970930 In: European journal of human genetics : EJHG vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	34.	Enzyme-linked immunosorbent assay of pS2 in breast cancers, benign tumors, and normal breast tissues. Correlation with prognosis and adjuvant hormone therapy. [electronic resource] by Predine, J Spyratos, F Prud'homme, J F Andrieu, C Hacene, K Brunet, M Pallud, C Milgrom, E Producer: 19920415 In: Cancer vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Cloning of a gene expressed in human breast cancer and regulated by estrogen in MCF-7 cells. [electronic resource] by Prud'homme, J F Fridlansky, F Le Cunff, M Atger, M Mercier-Bodart, C Pichon, M F Milgrom, E Producer: 19850326 In: DNA (Mary Ann Liebert, Inc.) vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	17 beta-Hydroxysteroid dehydrogenase activity in human breast epithelial cell and fibroblast cultures. [electronic resource] by Prud'homme, J F Malet, C Gompel, A Lalardrie, J P Ochoa, C Boue, A Mauvais-Jarvis, P Kuttenn, F Producer: 19840530 In: Endocrinology vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33. [electronic resource] by Baulac, S Gourfinkel-An, I Picard, F Rosenberg-Bourgin, M Prud'homme, J F Baulac, M Brice, A LeGuern, E Producer: 20001002 In: American journal of human genetics vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22. [electronic resource] by Fischer, J Urtizberea, J A Pavek, S Vandiedonck, C Bruls, T Saker, S Alkatip, Y Prud'homme, J F Weissenbach, J Producer: 19980925 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Penetrating wounds of the abdomen: analysis of 776 operative cases. [electronic resource] by Pridgen, J E Herff, A F Watkins, H O Halbert, D S D'Avila, R Crouch, D M Prud'homme, J L Producer: 19670803 In: Annals of surgery vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31. [electronic resource] by Baulac, S Picard, F Herman, A Feingold, J Genin, E Hirsch, E Prud'homme, J F Baulac, M Brice, A LeGuern, E Producer: 20010628 In: Annals of neurology vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 61 results.