Show items per page
Elements: 15
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
HLA variation reveals genetic continuity rather than population group structure in East Asia Di, Da; Sanchez-Mazas, Alicia 2014
add to browser selection
Association of adenosine receptor gene polymorphisms and in vivo adenosine A1 receptor binding in the human brain Hohoff, Christa; Garibotto, Valentina; Elmenhorst, David; Baffa, Anna; ... Bauer, Andreas 2014
add to browser selection
Mutations of DEPDC5 cause autosomal dominant focal epilepsies Ishida, Saeko; Picard, Fabienne; Rudolf, Gabrielle; Noé, Eric; ... Baulac, Stéphanie 2013
add to browser selection
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled Attar Cohen, Homa; Bedard, Karen; Migliavacca Voeffray, Eugenia Linda; Gagnebin, Maryline; ... Antonarakis, Stylianos 2012
add to browser selection
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele Radhakrishna, Uppala; Nath, Swapan K; McElreavey, Ken; Ratnamala, Uppala; ... Butler, Merlin G 2012
add to browser selection
Mapping cis- and trans-regulatory effects across multiple tissues in twins Nica, Alexandra; Buil Demur, Alfonso Alberto; Dima, Antigoni; Montgomery, Stephen; Dermitzakis, Emmanouil 2012
add to browser selection
Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing Ratnamala, Uppala; Lyle, Robert; Rawal, Rakesh; Singh, Raminder; ... Radhakrishna, Uppala 2011
add to browser selection
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program Simino, Jeannette; Shi, Gang; Kume, Rezart; Schwander, Karen; ... Rao, Dabeeru C 2011
add to browser selection
Positional identification of variants of Adamts16 linked to inherited hypertension Joe, Bina; Saad, Yasser; Dhindaw, Seema; Lee, Norman H.; ... Bouchard, Claude 2009
add to browser selection
Lymphoid enhancer factor-1 links two hereditary leukemia syndromes through core-binding factor alpha regulation of ELA2 Li, Feng-Qian; Person, Richard E; Takemaru, Ken-Ichi; Williams, Kayleen; ... Horwitz, Marshall 2004
add to browser selection
A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Ferreiro-girani, Ana; Monnier, Nicole; Romero, Norma B; Leroy, Jean-Paul; ... Guicheney, Pascale 2002
add to browser selection
MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity DeLozier-Blanchet, C; Haenggeli, Charles-Antoine; Bottani, Armand 1999
add to browser selection
Bone marrow transplantation as treatment for X-linked immunodeficiency with hyper-IgM. Bordigoni, P; Auburtin, B; Carret, A S; Schuhmacher, A; ... Sommelet, D 1998
add to browser selection
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval Ducros, A; Nagy, T; Alamowitch, S; Nibbio, A; ... Tournier-Lasserve, E 1996
add to browser selection
Structure linkage : and sequence of the two genes encoding the delta and gamma subunits of the nicotinic acetylcholine receptor Nef, P.; Mauron, Alex; Stalder Monney, Romaine; Alliod, C.; Ballivet, M. 1984