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	9581.	Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation. [electronic resource] by Milà, M Sànchez, A Badenas, C Brun, C Jiménez, D Villa, M P Castellví-Bel, S Estivill, X Producer: 19971119 In: Human genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9582.	Coexisting true hermaphroditism and partial hydatidiform mole developing metastatic gestational trophoblastic tumors. A case report. [electronic resource] by Shiina, Hiroko Oka, Kuniyuki Okane, Masato Tanno, Wataru Kawasaki, Tomoaki Nakayama, Masahiro Producer: 20030123 In: Virchows Archiv : an international journal of pathology vol. 441 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9583.	Mosaicism due to myeloid lineage restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting. [electronic resource] by Körmöczi, Günther F Dauber, Eva-Maria Haas, Oskar A Legler, Tobias J Clausen, Frederik B Fritsch, Gerhard Raderer, Markus Buchta, Christoph Petzer, Andreas L Schönitzer, Diether Mayr, Wolfgang R Gassner, Christoph Producer: 20071030 In: Blood vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9584.	Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS. [electronic resource] by Kinsler, Veronica A Thomas, Anna C Ishida, Miho Bulstrode, Neil W Loughlin, Sam Hing, Sandra Chalker, Jane McKenzie, Kathryn Abu-Amero, Sayeda Slater, Olga Chanudet, Estelle Palmer, Rodger Morrogh, Deborah Stanier, Philip Healy, Eugene Sebire, Neil J Moore, Gudrun E Producer: 20131031 In: The Journal of investigative dermatology vol. 133 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9585.	Penicillin-resistant viridans streptococci have obtained altered penicillin-binding protein genes from penicillin-resistant strains of Streptococcus pneumoniae. [electronic resource] by Dowson, C G Hutchison, A Woodford, N Johnson, A P George, R C Spratt, B G Producer: 19900904 In: Proceedings of the National Academy of Sciences of the United States of America vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9586.	[Intersexuality in childhood]. [electronic resource] by Knorr, D Producer: 19750416 In: Medizinische Klinik vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	9587.	Gene control of mammalian differentiation. [electronic resource] by Mintz, B Producer: 19750314 In: Annual review of genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9588.	Bone marrow transplantation incompatibility modified by F 1 graft inocula. [electronic resource] by Chee, C A Ilbery, P L Motta, R Producer: 19720911 In: Revue europeenne d'etudes cliniques et biologiques. European journal of clinical and biological research vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	9589.	Runting syndromes, autoimmunity, and neoplasia. [electronic resource] by Keast, D Producer: 19690619 In: Advances in cancer research vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9590.	Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation. [electronic resource] by Webb, A L Sturgiss, S Warwicker, P Robson, S C Goodship, J A Wolstenholme, J Producer: 19970227 In: Prenatal diagnosis vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9591.	A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males. [electronic resource] by Haddad, L A Mingroni-Netto, R C Vianna-Morgante, A M Pena, S D Producer: 19960712 In: Human genetics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9592.	vab-8 is a key regulator of posteriorly directed migrations in C. elegans and encodes a novel protein with kinesin motor similarity. [electronic resource] by Wolf, F W Hung, M S Wightman, B Way, J Garriga, G Producer: 19980602 In: Neuron vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9593.	Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction. [electronic resource] by Chen, Chih-Ping Chern, Schu-Rern Chang, Tung-Yao Lee, Chen-Chi Chen, Li-Feng Tzen, Chin-Yuan Wang, Wayseen Lin, Chen-Ju Yang, Brian P T Yang, Lawrence S T Producer: 20030702 In: Prenatal diagnosis vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9594.	Severe craniofacial malformations and deglutition dysfunction in a brother and sister: new syndrome? [electronic resource] by Orstavik, K H Tangsrud, S E Nordshus, T Lange, J E Renolen, O Lyberg, T Producer: 19980923 In: American journal of medical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9595.	A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA. [electronic resource] by Majamaa-Voltti, K A M Winqvist, S Remes, A M Tolonen, U Pyhtinen, J Uimonen, S Kärppä, M Sorri, M Peuhkurinen, K Majamaa, K Producer: 20060628 In: Neurology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9596.	Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept. [electronic resource] by Poblete-Gutiérrez, Pamela Wiederholt, Tonio König, Arne Jugert, Frank K Marquardt, Yvonne Rübben, Albert Merk, Hans F Happle, Rudolf Frank, Jorge Producer: 20041214 In: The Journal of clinical investigation vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9597.	Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies. [electronic resource] by Bashamboo, Anu Rahman, Mohammed Mahidur Prasad, Aparna Chandy, Sebastian Padinjarel Ahmad, Jamal Ali, Sher Producer: 20050706 In: Molecular human reproduction vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9598.	Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS. [electronic resource] by Hitchins, Megan P Rickard, Sarah Dhalla, Fatima Fairbrother, Una L de Vries, Bert B A Winter, Robin Pembrey, Marcus E Malcolm, Sue Producer: 20040928 In: American journal of medical genetics. Part A vol. 125A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9599.	Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. [electronic resource] by Nazlican, Hülya Zeschnigk, Michael Claussen, Uwe Michel, Susanne Boehringer, Stefan Gillessen-Kaesbach, Gabriele Buiting, Karin Horsthemke, Bernhard Producer: 20050517 In: Human molecular genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9600.	A large-scale validation of dosage analysis by robust dosage-polymerase chain reaction. [electronic resource] by Nguyen, Vu Q Liu, Qiang Sommer, Steve S Producer: 20071207 In: Analytical biochemistry vol. 371 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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