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	81.	Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiency. [electronic resource] by Bosson, D Kuhnle, U Mees, N Ramet, J Vamos, E Vertongen, F Wolter, R Armanini, D Producer: 19861125 In: Acta endocrinologica. Supplementum vol. 279 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings. [electronic resource] by Przedborski, S Ferster, A Goldman, S Wolter, R Song, M Tonnesen, T Pollitt, R J Vamos, E Producer: 19900607 In: American journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findings. [electronic resource] by de Vroede, M Feremans, W de Maertelaere-Laurent, E Mandelbaum, I Toppet, M Vamos, E Fondu, P Producer: 19821202 In: Scandinavian journal of haematology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	[Fetal cardiology: prenatal diagnosis of cardiac malformations]. [electronic resource] by Viart, P Rondia, G Dessy, H Gallez, A Deuvaert, F E Blum, D Heimann, P Vamos, E Producer: 19940203 In: Revue medicale de Bruxelles vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	85.	Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy. [electronic resource] by Steenhout, P Elmer, C Clercx, A Blum, D Gnat, D van Erum, S Vertongen, F Vamos, E Producer: 19900524 In: Journal of inherited metabolic disease vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Analysis of the peripheral T-cell compartment in the MHC class II deficiency syndrome. [electronic resource] by Lambert, M van Eggermond, M Andrien, M Mascart, F Vamos, E Dupont, E van den Elsen, P Producer: 19920409 In: Research in immunology vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Multiple clonal chromosome aberrations in a case of childhood focal nodular hyperplasia of the liver. [electronic resource] by Heimann, P Ogur, G Debusscher, C De Valck, C Sariban, E Deprez, C De Roy, G Vamos, E Producer: 19960222 In: Cancer genetics and cytogenetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	[Bone marrow graft in hereditary diseases]. [electronic resource] by Bujan, W Ferster, A Devalck, C Vamos, E Mascart, F Denis, R Azzi, N Vergauwen, P Sariban, E Producer: 19920820 In: Revue medicale de Bruxelles vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	89.	Neonatal multiple sulphatase deficiency disorder: biochemical characterization. [electronic resource] by Eto, Y Tokoro, T Kureha, Y Koda, N Tada, Y Tahara, T Maekawa, K Liebaers, I Vamos, E Producer: 19830610 In: Journal of inherited metabolic disease vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Migraine is a neuronal disease. [electronic resource] by Tajti, J Párdutz, A Vámos, E Tuka, B Kuris, A Bohár, Zs Fejes, A Toldi, J Vécsei, L Producer: 20120313 In: Journal of neural transmission (Vienna, Austria : 1996) vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Anaplastic large cell lymphoma of true histiocytic origin in an infant: unusual clinical, hematological, and cytogenetic features. [electronic resource] by Ferster, A Corazza, F Heimann, P Dehou, M F De Busscher, C Devalck, C Sariban, E Vamos, E Producer: 19940119 In: Medical and pediatric oncology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Lethal osteopetrosis with multiple fractures in utero. [electronic resource] by el Khazen, N Faverly, D Vamos, E Van Regemorter, N Flament-Durand, J Carton, B Cremer-Perlmutter, N Producer: 19860403 In: American journal of medical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	C heterochromatin variation in couples with recurrent early abortions. [electronic resource] by Maes, A Staessen, C Hens, L Vamos, E Kirsch-Volders, M Lauwers, M C Defrise-Gussenhoven, E Susanne, C Producer: 19840107 In: Journal of medical genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	Cordocentesis for rapid karyotype: 421 consecutive cases. [electronic resource] by Donner, C Rypens, F Paquet, V Cohen, E Delneste, D van Regemorter, N Vamos, E Avni, F Rodesch, F Producer: 19950921 In: Fetal diagnosis and therapy vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts. [electronic resource] by Telerman-Toppet, N Biarent, D Bouton, J M de Meirleir, L Elmer, C Noel, S Vamos, E DiMauro, S Producer: 19921116 In: Journal of inherited metabolic disease vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Congenital malformations in 10,000 consecutive births in a university hospital: need for genetic counseling and prenatal diagnosis. [electronic resource] by Van Regemorter, N Dodion, J Druart, C Hayez, F Vamos, E Flament-Durand, J Perlmutter-Cremer, N Rodesch, F Producer: 19840502 In: The Journal of pediatrics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	97.	[Prenatal diagnosis of malformations of the central nervous system]. [electronic resource] by Elkhazen, N Dodion, J Vamos, E Vanregemorter, N Spehl, M Perlmutter, N Rodesch, F Depierreux, M Flament-Durand, J Producer: 19840723 In: Journal de gynecologie, obstetrique et biologie de la reproduction vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	98.	Severe Smith-Lemli-Opitz syndrome with prolonged survival and lipid abnormalities. [electronic resource] by Pierquin, G Peeters, P Roels, F Vamos, E Brucher, J M Tint, G S Honda, A Van Regemorter, N Producer: 19950711 In: American journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Hyperphosphatasemia in early diagnosed infantile GM1 gangliosidosis presenting as transient hydrops fetalis. [electronic resource] by Denis, R Wayenberg, J L Vermeulen, M Gorus, F Gerlo, E Lissens, W Liebaers, I Jauniaux, E Vamos, E Producer: 19970103 In: Acta clinica Belgica vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer. [electronic resource] by Amfo, K Neyns, B Teugels, E Lissens, W Bourgain, C De Sutter, P Vandamme, B Vamos, E De Grève, J Producer: 19950831 In: Oncogene vol. 11 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 122 results.