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	1.	Episphalosomic syndrome : a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens. [electronic resource] by Verloes, A Jamar, M Dideberg, V Herens, C Producer: 20011204 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic risk in natural and medically assisted procreation. [electronic resource] by Koulischer, L Verloes, A Lesenfants, S Jamar, M Herens, C Producer: 19990415 In: Early pregnancy : biology and medicine : the official journal of the Society for the Investigation of Early Pregnancy vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	3.	GOMBO syndrome: another "pseudorecessive" disorder due to a cryptic translocation. [electronic resource] by Verloes, A Lesenfants, S Jamar, M Dideberg, V Herens, C Producer: 20010104 In: American journal of medical genetics vol. 95 Availability: No items available. Save to lists Add to cart (remove)
	4.	A low rate of trisomy 21 in twin-pregnancies: a cytogenetics retrospective study of 278 cases. [electronic resource] by Jamar, M Lemarchal, C Lemaire, V Koulischer, L Bours, V Producer: 20040421 In: Genetic counseling (Geneva, Switzerland) vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	5.	Inv(12)(q15q24): a nonrandom change associated with myelodysplasia? [electronic resource] by Scantamburlo, G Lampertz, S Croisiau, C Jamar, M Koulischer, L Herens, C Producer: 20001204 In: Cancer genetics and cytogenetics vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia. [electronic resource] by Herens, C Brasseur, E Jamar, M Vierset, L Schoenen, I Koulischer, L Producer: 19990527 In: Clinical and laboratory haematology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Precocious puberty associated with partial trisomy 18q and monosomy 11q. [electronic resource] by Mutesa, L Hellin, A C Jamar, M Pierquin, G Bours, V Verloes, A Producer: 20071016 In: Genetic counseling (Geneva, Switzerland) vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	8.	[Fish and chips]. [electronic resource] by Delvenne, P Deprez, M Bisig, B Jamar, M Boniver, J Bours, V Herens, Ch Producer: 20110329 In: Revue medicale de Liege vol. 65 Spec no. Availability: No items available. Save to lists Add to cart (remove)
	9.	Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes. [electronic resource] by Riegel, M Baumer, A Jamar, M Delbecque, K Herens, C Verloes, A Schinzel, A Producer: 20011207 In: Human genetics vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association. [electronic resource] by Verloes, A Curry, C Jamar, M Herens, C O'Lague, P Marks, J Sarda, P Blanchet, P Producer: 19990204 In: Journal of medical genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Cytogenetic study of bovine oocytes matured in vitro. [electronic resource] by Ectors, F J Koulischer, L Jamar, M Herens, C Verloes, A Remy, B Beckers, J F Producer: 20070717 In: Theriogenology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome. [electronic resource] by Mutesa, L Vanbellinghen, J F Hellin, A C Segers, K Jamar, M Pierquin, G Bours, V Producer: 20090602 In: Genetic counseling (Geneva, Switzerland) vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	13.	Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13. [electronic resource] by Uwineza, A Pierquin, G Gaillez, S Jamar, M Hellin, A C Caberg, J H Bours, V Producer: 20131018 In: Genetic counseling (Geneva, Switzerland) vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	14.	Monosomy 11q: report of two familial cases and review of the literature. [electronic resource] by Hustinx, R Verloes, A Grattagliano, B Herens, C Jamar, M Soyeur, D Schaaps, J P Koulischer, L Producer: 19940419 In: American journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome. [electronic resource] by Herens, C Jamar, M Alvarez-Gonzalez, M L Lesenfants, S Lombet, J Bonnivert, J Koulischer, L Verloes, A Producer: 19980212 In: American journal of medical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test? [electronic resource] by Verloes, A Gillerot, Y Van Maldergem, L Schoos, R Herens, C Jamar, M Dideberg, V Lesenfants, S Koulischer, L Producer: 20010405 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis. [electronic resource] by Herens, C Hermanne, J P Tassin, F Fassotte, M F Thiry, A Jamar, M Schaaf-Lafontaine, N Fillet, G Koulischer, L Producer: 19990421 In: Cancer genetics and cytogenetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)