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	101.	Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly. [electronic resource] by Courtens, W Tjalma, W Messiaen, L Vamos, E Martin, J J Van Bogaert, E Keersmaekers, G Meulyzer, P Wauters, J Producer: 19980709 In: American journal of medical genetics vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	102.	Prenatal diagnosis and confirmation of infantile sialic acid storage disease. [electronic resource] by Vamos, E Libert, J Elkhazen, N Jauniaux, E Hustin, J Wilkin, P Baumkötter, J Mendla, K Cantz, M Strecker, G Producer: 19870304 In: Prenatal diagnosis vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Clinical and cytogenetic studies of two cases of Klinefelter syndrome with hereditary retinoblastoma and rhabdomyosarcoma. [electronic resource] by Oğur, G Sengun, Z Arel-Kiliç, G De Busscher, C Başaran, S Ozbek, U Ayan, I Sariban, E Vamos, E Producer: 19960829 In: Cancer genetics and cytogenetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus. [electronic resource] by Abramowicz, M J Andrien, M Dupont, E Dorchy, H Parma, J Duprez, L Ledley, F D Courtens, W Vamos, E Producer: 19940819 In: The Journal of clinical investigation vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	[Cordocentesis: experience in 391 initial samples]. [electronic resource] by Donner, C Simon, P Gosselin, F Vermeylen, D Avni, F Liesnard, C Vamos, E Cochaux, P Vassart, G Rodesch, F Producer: 19900823 In: Revue medicale de Bruxelles vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	106.	[Prenatal diagnosis of malformations of the central nervous system]. [electronic resource] by el Khazen, N Dodion, J Vamos, E Vanregemorter, N Spehl, M Perlmutter, N Rodesch, F Depierreux, M Flament-Durand, J Producer: 19841101 In: Revue medicale de Bruxelles vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	107.	Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. [electronic resource] by Sermon, K Henderix, P Lissens, W De Vos, A Vandervorst, M Vanderfaeillie, A Vamos, E Van Steirteghem, A Liebaers, I Producer: 20010222 In: Molecular human reproduction vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Pyruvate dehydrogenase deficiency: clinical and biochemical diagnosis. [electronic resource] by De Meirleir, L Lissens, W Denis, R Wayenberg, J L Michotte, A Brucher, J M Vamos, E Gerlo, E Liebaers, I Producer: 19930922 In: Pediatric neurology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome. [electronic resource] by Pierquin, G Van Regemorter, N Fourneau, C Bormans, J Foerster, M Damis, E Cremer-Perlmutter, N Lapiere, C M Vamos, E Producer: 19911030 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-oxoprolinase deficiency. [electronic resource] by Cohen, L H Vamos, E Heinrichs, C Toppet, M Courtens, W Kumps, A Mardens, Y Carlsson, B Grillner, L Larsson, A Producer: 19980210 In: European journal of pediatrics vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Congenital absence of insulin cells in a neonate with diabetes mellitus and mutase-deficient methylmalonic acidaemia. [electronic resource] by Blum, D Dorchy, H Mouraux, T Vamos, E Mardens, Y Kumps, A De Prez, C Heimann, P Fowler, B Baumgartner, R Producer: 19930524 In: Diabetologia vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Pathological pregnancies. Results of amniotic fluid studies and fetal outcome. [electronic resource] by Van Regemorter, N Vamos, E Defleur, V el Khazen, N Jeanty, P Levi, S Avni, F Foulon, W Liebaers, I Rodesch, F Producer: 19860703 In: Acta obstetricia et gynecologica Scandinavica vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	[Attempt at antenatal diagnosis of argininosuccinic aciduria]. [electronic resource] by Dhondt, J L Farriaux, J P Pollitt, R J Vamos, E Richard, P Blanckaert, D Delecour, M Monnier, J C Fontaine, G Producer: 19760802 In: Annales de genetique vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	114.	[Medical genetics service]. [electronic resource] by Vassart, G Abramowicz, M Cochaux, P Duprez, L el Housni, H Hayez, F Heimann, P Parma, J Vamos, E Van Regemorter, N Producer: 20030515 In: Revue medicale de Bruxelles vol. 23 Suppl 2 Availability: No items available. Save to lists Add to cart (remove)
	115.	Collaborative study of the molecular epidemiology of Tay-Sachs disease in Europe. [electronic resource] by Akli, S Boue, J Sandhoff, K Kleijer, W Vamos, E Young, E Gatti, R Di Natale, P Motte, J Vanier, M T Producer: 19940831 In: European journal of human genetics : EJHG vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Severe congenital cutis laxa with pulmonary emphysema: a family with three affected sibs. [electronic resource] by Van Maldergem, L Vamos, E Liebaers, I Petit, P Vandevelde, G Simonis-Blumenfrucht, A Bouffioux, R Kulakowski, S Hanquinet, S Van Durme, P Producer: 19890420 In: American journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome. [electronic resource] by Davies, A F Olavesen, M G Stephens, R J Davidson, R Delneste, D Van Regemorter, N Vamos, E Flinter, F Abusaad, I Ragoussis, J Producer: 19961015 In: Human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion. [electronic resource] by Courtens, W Grossman, D Van Roy, N Messiaen, L Vamos, E Toppet, V Haumont, D Streydio, C Jauch, A Vermeesch, J R Speleman, F Producer: 19981223 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Delineation of two distinct 6p deletion syndromes. [electronic resource] by Davies, A F Mirza, G Sekhon, G Turnpenny, P Leroy, F Speleman, F Law, C van Regemorter, N Vamos, E Flinter, F Ragoussis, J Producer: 19990316 In: Human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	120.	Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA. [electronic resource] by Tritschler, H J Andreetta, F Moraes, C T Bonilla, E Arnaudo, E Danon, M J Glass, S Zelaya, B M Vamos, E Telerman-Toppet, N Producer: 19920302 In: Neurology vol. 42 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 122 results.