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	1.	Molecular analysis of a complex chromosomal rearrangement and a review of familial cases. [electronic resource] by Batista, D A Pai, G S Stetten, G Producer: 19950310 In: American journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Tetrasomy 18p: tentative delineation of a syndrome. [electronic resource] by Batista, D A Vianna-Morgante, A M Richieri-Costa, A Producer: 19830617 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)
	3.	An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line. [electronic resource] by Batista, D A Escallon, C Blakemore, K J Stetten, G Producer: 19950720 In: Prenatal diagnosis vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization. [electronic resource] by Chen, H Tuck-Muller, C M Batista, D A Wertelecki, W Producer: 19950828 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)
	5.	Duplication of the short arm of the X chromosome in mother and daughter. [electronic resource] by Tuck-Muller, C M Martinez, J E Batista, D A Kearns, W G Wertelecki, W Producer: 19930701 In: Human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization. [electronic resource] by Batista, D A Tuck-Muller, C M Martinez, J E Kearns, W G Pearson, P L Stetten, G Producer: 19931012 In: Human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Myoclonus-dystonia and Silver-Russell syndrome resulting from maternal uniparental disomy of chromosome 7. [electronic resource] by Sheridan, M B Bytyci Telegrafi, A Stinnett, V Umeh, C C Mari, Z Dawson, T M Bodurtha, J Batista, D A S Producer: 20140408 In: Clinical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Acute bilineal leukemia: a rare disease with poor outcome. [electronic resource] by Weir, E G Ali Ansari-Lari, M Batista, D A S Griffin, C A Fuller, S Smith, B D Borowitz, M J Producer: 20071211 In: Leukemia vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins. [electronic resource] by Doheny, K F Rasmussen, S A Rutberg, J Semenza, G L Stamberg, J Schwartz, M Batista, D A Stetten, G Thomas, G H Producer: 19970508 In: American journal of medical genetics vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	10.	Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. [electronic resource] by Tuck-Muller, C M Chen, H Martínez, J E Shen, C C Li, S Kusyk, C Batista, D A Bhatnagar, Y M Dowling, E Wertelecki, W Producer: 19950817 In: Human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Loss of the mismatched human leukocyte antigen haplotype in two acute myelogenous leukemia relapses after haploidentical bone marrow transplantation with post-transplantation cyclophosphamide. [electronic resource] by McCurdy, S R Iglehart, B S Batista, D A Gocke, C D Ning, Y Knaus, H A Jackson, A M Leffell, M S Luznik, L Gojo, I Producer: 20180309 In: Leukemia vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy? [electronic resource] by Nowaczyk, M J M Thompson, B A Zeesman, S Moog, U Sanchez-Lara, P A Magoulas, P L Falk, R E Hoover-Fong, J E Batista, D A S Amudhavalli, S M White, S M Graham, G E Rauen, K A Producer: 20150330 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)