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	21.	Trisomy 10p due to a de novo t(10p;13p). [electronic resource] by Aller, V Abrisqueta, J A Pérez-Castillo, A del Mazo, J Martín-Lucas, M A de Torres, M L Producer: 19790523 In: Human genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	An r(22)(p11 leads to q13) in a moderately mentally retarded girl. [electronic resource] by Aller, V Abrisqueta, J A de Torres, M L Martín-Lucas, M A Pérez-Castillo, A Del Mazo, J Producer: 19800215 In: Human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	The 18p- syndrome. Report of five cases. [electronic resource] by Zumel, R M Darnaude, M T Delicado, A Diaz de Bustamante, A de Torres, M L López-Pájares, I Producer: 19891201 In: Annales de genetique vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	24.	Tetrasomy 8p: discordance of amniotic fluid and blood karyotypes. [electronic resource] by López-Pajares, I Delicado, A Lapunzina, P Mori, M A De Torres, M L Aso, S Garcia Sanchez, P Producer: 20031128 In: American journal of medical genetics. Part A vol. 118A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Partial deletion of 4p16 band in a ring chromosome and Wolf Syndrome. [electronic resource] by del Mazo, J Abrisqueta, J A Pérez-Castillo, A Aller, V Lucas, M A de Torres, M L Martín, M J Producer: 19790124 In: Human genetics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	[Balanced translocation 8:10 and adrenogenital syndrome. Family study (author's transl)]. [electronic resource] by del Mazo, J Martín, M J Abrisqueta, J A Aller, V Martín-Lucas, M A Pérez-Castillo, A de Torres, M L Producer: 19810126 In: Anales espanoles de pediatria vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	27.	Balanced reciprocal translocation (X;20) limited to Wilms' tumor in a Wiedemann-Beckwith syndrome. [electronic resource] by Diaz de Bustamante, A Delicado, A Garcia de Miguel, P Darnaude, M T de Torres, M L Zumel, R M Lopez Pajares, I Producer: 19900326 In: Cancer genetics and cytogenetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Partial trisomy 13 due to maternal translocation t(7;13)(p22q14). [electronic resource] by Martin-Lucas, M A Pérez-Castillo, A Abrisqueta, J A de Torres, M L Martin-Sempere, M J Del Mazo, J Aller, V Producer: 19821218 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	29.	Euchromatic variant 16p+. Implications in prenatal diagnosis. [electronic resource] by López Pajares, I Villa, O Salido, M Mori, M A Gonzalez, A Lapunzina, P De Torres, M L Vallcorba, I Palomares, M Fernández, L Delicado, A Producer: 20061201 In: Prenatal diagnosis vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Unusual four-generation chromosome-22 rearrangement: when "normality" masks abnormality. [electronic resource] by Nevado, Julián de Torres, M Luisa Fernández, Luis Mori, M Angeles Villa, Amelia Palomares, María García-Santiago, Fe Mansilla, Elena García-Miñaur, Sixto Delicado, Alicia Lapunzina, Pablo Producer: 20090923 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome. [electronic resource] by Fernández, L Lapunzina, P Arjona, D López Pajares, I García-Guereta, L Elorza, D Burgueros, M De Torres, M L Mori, M A Palomares, M García-Alix, A Delicado, A Producer: 20051020 In: Clinical genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Customized high resolution CGH-array for clinical diagnosis reveals additional genomic imbalances in previous well-defined pathological samples. [electronic resource] by Vallespín, Elena Palomares Bralo, María Mori, M Ángeles Martín, Rubén García-Miñaúr, Sixto Fernández, Luis de Torres, M Luisa García-Santiago, Fe Mansilla, Elena Santos, Fernando M-Montaño, Victoria E Crespo, M Carmen Martín, Sol Martínez-Glez, Victor Delicado, Alicia Lapunzina, Pablo Nevado, Julián Producer: 20131017 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)