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	221.	Maternal 47,XX,i(X)(q10) as a cause of false positive sex chromosome aneuploidy in noninvasive prenatal screening. [electronic resource] by DeMaio, Alison Green, Andrew Daly, Sean Producer: 20170831 In: Prenatal diagnosis vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	222.	Chronic lymphocytic leukemia with isochromosome 17q: An aggressive subgroup associated with TP53 mutations and complex karyotypes. [electronic resource] by Collado, Rosa Puiggros, Anna López-Guerrero, José Antonio Calasanz, Ma José Larráyoz, Ma José Ivars, David García-Casado, Zaida Abella, Eugènia Orero, Ma Teresa Talavera, Elisabet Oliveira, Ana Carla Hernández-Rivas, Jesús Ma Hernández-Sánchez, María Luño, Elisa Valiente, Alberto Grau, Javier Portal, Inmaculada Gardella, Santiago Salgado, Anna Camino Giménez, Ma Teresa Ardanaz, Ma Teresa Campeny, Andrea Hernández, José Julio Álvarez, Sara Espinet, Blanca Carbonell, Félix Producer: 20171020 In: Cancer letters vol. 409 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	223.	Mild phenotype in a 15-year-old boy with Pallister-Killian syndrome. [electronic resource] by Genevieve, D Cormier-Daire, V Sanlaville, D Faivre, L Gosset, P Allart, L Picq, M Munnich, A Romana, S de Blois, Mc Vekemans, M Producer: 20030530 In: American journal of medical genetics. Part A vol. 116A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	224.	Identification of the critical region of 12p over-representation in testicular germ cell tumors of adolescents and adults. [electronic resource] by Mostert, M C Verkerk, A J van de Pol, M Heighway, J Marynen, P Rosenberg, C van Kessel, A G van Echten, J de Jong, B Oosterhuis, J W Looijenga, L H Producer: 19980629 In: Oncogene vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	225.	Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q-). [electronic resource] by Li, Tianyu Xue, Yongquan Wu, Yafang Pan, Jinlan Producer: 20040604 In: British journal of haematology vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	226.	45,X/46,XX karyotype mitigates the aberrant craniofacial morphology in Turner syndrome. [electronic resource] by Rizell, Sara Barrenäs, Marie-Louise Andlin-Sobocki, Anna Stecksén-Blicks, Christina Kjellberg, Heidrun Producer: 20140521 In: European journal of orthodontics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	227.	Isochromosome 17q10 associated with basophilia in primary myelofibrosis while with JAK2 inhibitor. [electronic resource] by Koumas, S Prokopiou, C Lerni, M Seimeni, O Neokleous, N Producer: 20150909 In: Annals of hematology vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	228.	Pallister-Killian syndrome presenting through nuchal translucency screening for trisomy 21. [electronic resource] by Langford, K Hodgson, S Seller, M Maxwell, D Producer: 20000907 In: Prenatal diagnosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q). [electronic resource] by Björck, E J Anderlid, B M Blennow, E Producer: 19991201 In: American journal of medical genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	230.	Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus. [electronic resource] by Chen, C P Chern, S R Lee, C C Chen, L F Chuang, C Y Chen, M H Producer: 19980717 In: Prenatal diagnosis vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	231.	Two cases of tetrasomy 9p syndrome with tissue limited mosaicism. [electronic resource] by Lloveras, Elisabet Pérez, C Solé, F Zamora, L Lladonosa, A Espinet, B Silvestre, E Serra, J Vendrell, T Fernández, B Salido, M Plaja, A Producer: 20040916 In: American journal of medical genetics. Part A vol. 124A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	232.	Prenatal diagnosis and characterization of an analphoid marker chromosome 16. [electronic resource] by Tabet, A C Gosset, P Elghezal, H Fontaine, S Martinovic, J Encha Razavi, F Romana, S Vekemans, M Morichon-Delvallez, N Producer: 20050308 In: Prenatal diagnosis vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	233.	Sonographic appearance of ovaries and gonadotropin secretions as prognostic tools of spontaneous puberty in girls with Turner's syndrome. [electronic resource] by Matarazzo, P Lala, R Artesani, L Franceshini, P G De Sanctis, C Producer: 19961112 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	234.	Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization. [electronic resource] by Darnaude, M T Diaz de Bustamante, A Cabello, P Vallcorba, I Producer: 19961107 In: Annales de genetique vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	235.	Pallister-Killian syndrome: case report with pineal tumor. [electronic resource] by Mauceri, L Sorge, G Incorpora, G Pavone, L Producer: 20001130 In: American journal of medical genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	236.	Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q. [electronic resource] by Breman, Amy M Probst, Frank J Blazo, Maria A Schaaf, Christian P Roney, Erin K Craigen, William J Bacino, Carlos A Cheung, Sau Wai Producer: 20110920 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	237.	Trisomy 13 due to rea(13q;13q) is caused by i(13) and not rob(13;13)(q10;q10) in the majority of cases. [electronic resource] by Bugge, Merete deLozier-Blanchet, Celia Bak, Mads Brandt, Carsten A Hertz, Jens Michael Nielsen, Jytte Bieber Duprez, Laurance Petersen, Michael B Producer: 20050315 In: American journal of medical genetics. Part A vol. 132A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	238.	Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes. [electronic resource] by Saunders, K Czepulkowski, B Sivalingam, R Hayes, J P L A Aldouri, M Sekhar, M Cummins, M Ho, A Mufti, G J Producer: 20050413 In: Cancer genetics and cytogenetics vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	239.	Goldenhar syndrome and medulloblastoma: a coincidental association? The first case report. [electronic resource] by Aizenbud, Dror Shoham, Natasha V Constantini, Shlomi Nevo, Neta Ben Arush, Myriam Raz, Michal Rachmiel, Adi Goldsher, Dorit Producer: 20150630 In: Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	240.	Significance of chromosome 5 and 17 changes in the development of carcinoma of the cervix uteri. [electronic resource] by Atkin, N B Producer: 20010329 In: Cytogenetics and cell genetics vol. 91 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 438 results.