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	21.	First report of congenital adrenal cysts and pheochromocytoma in a patient with mosaic genome-wide paternal uniparental disomy. [electronic resource] by White, Mary McGillivray, George White, Sue M Zacharin, Margaret R Producer: 20180129 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	A study of voice and non-voice processing in Prader-Willi syndrome. [electronic resource] by Strenilkov, Kuzma Debladis, Jimmy Salles, Juliette Valette, Marion Mantoulan, Carine Thuilleaux, Denise Laurier, Virginie Molinas, Catherine Barone, Pascal Tauber, Maïthé Producer: 20210618 In: Orphanet journal of rare diseases vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Supernumerary marker chromosomes (SMC) and uniparental disomy (UPD): coincidence or consequence? [electronic resource] by Kotzot, D Producer: 20021213 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Case Report of Infant With Features of Beckwith-Wiedemann Syndrome Diagnosed With Genome-wide Uniparental Disomy. [electronic resource] by Reed, Jennifer A Crotwell, Patricia L Stein, Quinn Mroch, Amy Davis-Keppen, Laura Khan, Akram Producer: 20190426 In: South Dakota medicine : the journal of the South Dakota State Medical Association vol. 70 Availability: No items available. Save to lists Add to cart (remove)
	25.	Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations. [electronic resource] by Berend, Sue Ann Bejjani, Bassem A McCaskill, Christopher Shaffer, Lisa G Producer: 20030210 In: American journal of medical genetics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns. [electronic resource] by Rivolta, Carlo Sharon, Dror DeAngelis, Margaret M Dryja, Thaddeus P Producer: 20021113 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Production of haploid and diploid androgenetic zebrafish. [electronic resource] by Brandhorst, Bruce P Corley-Smith, Graham E Producer: 20040719 In: Methods in molecular biology (Clifton, N.J.) vol. 254 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation. [electronic resource] by Garelli, Emanuela Quarello, Paola Giorgio, Elisa Carando, Adriana Menegatti, Elisa Mancini, Cecilia Di Gregorio, Eleonora Crescenzio, Nicoletta Palumbo, Orazio Carella, Massimo Dimartino, Paola Pippucci, Tommaso Dianzani, Irma Ramenghi, Ugo Brusco, Alfredo Producer: 20200612 In: British journal of haematology vol. 185 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Segmental uniparental disomy of 7q31-qter is rare in Silver-Russell syndrome. [electronic resource] by Eggermann, T Mergenthaler, S Eggermann, K Ranke, M B Wollmann, H A Producer: 20020508 In: Clinical genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature. [electronic resource] by Powis, Z Erickson, R P Producer: 20091102 In: Journal of applied genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	21 TRISOMY/NORMAL MOSAICISM IN AN INTELLIGENT CHILD WITH SOME MONGOLOID CHARACTERS. [electronic resource] by CLARKE, C M FORD, C E EDWARDS, J H SMALLPEICE, V Producer: 19961201 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Non-chromosome 15 marker chromosome in a Prader-Willi syndrome patient with uniparental disomy. [electronic resource] by Ichikawa, Mizuho Okajima, Maki Wada, Takahito Gokan, Yumi Shimakage, Hiromi Tonoki, Hidefumi Saitoh, Shinji Producer: 20060609 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	[(Epi) genetic mechanisms leading to imprinting disorder]. [electronic resource] by Ogata, Tsutomu Producer: 20151026 In: No to hattatsu = Brain and development vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	34.	[Monogenic hereditary diseases]. [electronic resource] by Jensen, Peter K A Producer: 20030416 In: Ugeskrift for laeger vol. 165 Availability: No items available. Save to lists Add to cart (remove)
	35.	Mother-child exclusion due to paternal uniparental disomy 6. [electronic resource] by Wegener, R Weirich, V Dauber, E M Mayr, W R Producer: 20070208 In: International journal of legal medicine vol. 120 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Silver-Russell syndrome in a patient with somatic mosaicism for upd(11)mat identified by buccal cell analysis. [electronic resource] by Luk, Ho-Ming Ivan Lo, Fai-Man Sano, Shinichiro Matsubara, Keiko Nakamura, Akie Ogata, Tsutomu Kagami, Masayo Producer: 20180129 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Chromosomes and clinical anatomy. [electronic resource] by Gardner, Robert James McKinlay Producer: 20170206 In: Clinical anatomy (New York, N.Y.) vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Extreme hypertriglyceridemia, pseudohyponatremia, and pseudoacidosis in a neonate with lipoprotein lipase deficiency due to segmental uniparental disomy. [electronic resource] by Ashraf, Ambika P Hurst, Anna C E Garg, Abhimanyu Producer: 20171226 In: Journal of clinical lipidology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	The relationship of JAK2(V617F) and acquired UPD at chromosome 9p in polycythemia vera. [electronic resource] by Wang, L Swierczek, S I Lanikova, L Kim, S J Hickman, K Walker, K Wang, K Drummond, J Doddapaneni, H Reid, J G Muzny, D M Gibbs, R A Wheeler, D A Prchal, J T Producer: 20140616 In: Leukemia vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Persistent congenital hyperinsulinism in two patients with Beckwith-Wiedemann syndrome due to mosaic uniparental disomy 11p. [electronic resource] by Zarate, Yuri A Shur, Natasha Robin, Andrew Garnica, Adolfo D Quintos, Jose Bernardo Schaefer, G Bradley Producer: 20150525 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 27 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 1009 results.