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Results 1 to 25 of 21534

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9q34.3 deletion syndrome in three unrelated childrenIWAKOSHI, Mie; OKAMOTO, Nobuhiko; HARADA, Naoki et al.American journal of medical genetics. 2004, Vol 124A, Num 3, pp 278-283, issn 0148-7299, 6 p.Article

Molecular Mechanisms in 22q11 Deletion SyndromeWILLIAMS, Nigel M.Schizophrenia bulletin. 2011, Vol 37, Num 5, pp 882-889, issn 0586-7614, 8 p.Article

Fully dynamic algorithms for maintaining extremal sets in a family of setsHONG SHEN.International journal of computer mathematics. 1998, Vol 69, Num 3-4, pp 203-215, issn 0020-7160Article

Search for somatic 22q11.2 deletions in patients with conotruncal heart defectsRAUCH, Anita; HOFBECK, Michael; CESNJEVAR, Robert et al.American journal of medical genetics. 2004, Vol 124A, Num 2, pp 165-169, issn 0148-7299, 5 p.Article

Nucleotide deletion in RHCE*cE (907delC) is responsible for a D― ― haplotype in HispanicsWESTHOFF, Connie M; VEGE, Sunitha; NICKLE, Pam et al.Transfusion (Philadelphia, PA). 2011, Vol 51, Num 10, pp 2142-2147, issn 0041-1132, 6 p.Article

A new DEL variant caused by exon 8 deletionRICHARD, Martine; PERREAULT, Josée; CONSTANZO-YANEZ, Jessica et al.Transfusion (Philadelphia, PA). 2007, Vol 47, Num 5, pp 852-857, issn 0041-1132, 6 p.Article

Psychopathology in 22q11 deletion syndromeREIERSEN, Angela M; VORSTMAN, Jacob A. S; MORCUS, Monique E. J et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2007, Vol 46, Num 8, pp 942-944, issn 0890-8567, 3 p.Article

Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanismsCHEN, Jian-Min; FICHOU, Yann; JAMET, Déborah et al.Transfusion (Philadelphia, PA). 2013, Vol 53, Num 1, pp 206-210, issn 0041-1132, 5 p.Article

Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1ISHIHARA, N; YAMADA, K; MIMAKI, M et al.Journal of medical genetics. 2004, Vol 41, Num 5, pp 387-393, issn 0022-2593, 7 p.Article

Rapid Deletion-Based Subtyping System for the Manila Family of Mvcobacterium tuberculosisFRINK, Stephen; LISHI QIAN; STEVEN YU et al.Journal of clinical microbiology (Print). 2011, Vol 49, Num 5, pp 1951-1955, issn 0095-1137, 5 p.Article

Dynamic storage fragmentation and file deteriorationLEUNG, C. H. C.IEEE transactions on software engineering. 1986, Vol 12, Num 3, pp 436-441, issn 0098-5589Article

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndromeFERNANDEZ, Thomas; MORGAN, Thomas; DAVIS, Nicole et al.American journal of human genetics. 2004, Vol 74, Num 6, pp 1286-1293, issn 0002-9297, 8 p.Article

Markerless Gene Deletion System for SphingomonadsKACZMARCZYK, Andreas; VORHOLT, Julia A; FRANCEZ-CHARLOT, Anne et al.Applied and environmental microbiology (Print). 2012, Vol 78, Num 10, pp 3774-3777, issn 0099-2240, 4 p.Article

La délétion homozygote du gène DPY19L2 est responsable de la majorité des cas de globozoospermie = Homozygous deletion of DPY19L2 is responsible for most cases of globozoospermiaRAY, Pierre F; ARNOULT, Christophe.MS. Médecine sciences. 2011, Vol 27, Num 8-9, pp 692-693, issn 0767-0974, 2 p.Article

Application of high throughput cell array technology to FISH : Investigation of the role of deletion of p16 gene in leukemiasDONG SOON LEE; JEE HYUNG LEE; HYUN CHUNG MIN et al.Journal of biotechnology. 2007, Vol 127, Num 3, pp 355-360, issn 0168-1656, 6 p.Article

Neurexin 1 (NRXN1 ) Deletions in SchizophreniaKIROV, George; RUJESCU, Dan; INGASON, Andres et al.Schizophrenia bulletin. 2009, Vol 35, Num 5, pp 851-854, issn 0586-7614, 4 p.Article

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup NFERNANDES, S; PARACCHINI, S; MEYER, L. H et al.American journal of human genetics. 2004, Vol 74, Num 1, pp 180-187, issn 0002-9297, 8 p.Article

Swapping of functional domains using a chimeric monster deletion mutagenesis strategyYANG, Ching-Hui; ZWIEB, Christian.BioTechniques. 2001, Vol 31, Num 4, pp 724-728, issn 0736-6205, 3 p.Article

The pro region of human neutrophil defensin contains a motif that is essential for normal subcellular sortingLIDE LIU; GANZ, T.Blood. 1995, Vol 85, Num 4, pp 1095-1103, issn 0006-4971Article

Interstitial deletion of long arm of chromosome 13CARNEVALE, A; FRIAS, S; ALCANTAR, R et al.Annales de génétique (Paris). 1984, Vol 27, Num 1, pp 49-52, issn 0003-3995Article

Nasal abnormalities in the 9p deletion syndromeCERONI COMPADRETTI, Giacomo; TASCA, Ignazio; BARONCINI, Anna et al.Archives of otolaryngology, head & neck surgery. 2007, Vol 133, Num 10, pp 1054-1056, issn 0886-4470, 3 p.Article

In-frame triplet deletions in RHD alter the D antigen phenotypeFLEGEL, Willy A; EICHER, Nicole I; SCHREZENMEIER, Hubert et al.Transfusion (Philadelphia, PA). 2006, Vol 46, Num 12, pp 2156-2161, issn 0041-1132, 6 p.Article

Low incidence of deletion of the esterase D locus in retinoblastoma patientsDRYJA, T. P; BRUNS, G. A. P; GALLIE, B et al.Human genetics. 1983, Vol 64, Num 2, pp 151-155, issn 0340-6717Article

Spontaneous deletion mutation of soil-borne wheat mosaic virus RNA IISHIRAKO, Y; BRAKKE, M. K.Journal of general virology. 1984, Vol 65, Num 4, pp 855-858, issn 0022-1317Article

Das 13q ― Syndrom ― Die partielle Monosomie für den distalen Abschnitt des langen Armes des Chromosom 13 = Le syndrome 13q ― La monosomie partielle pour la partie distale du bras long du chromosome 13MÜCKE, J; SANDIG, K.-R; TRAUTMANN, U et al.Klinische Pädiatrie. 1983, Vol 195, Num 5, pp 361-364, issn 0300-8630Article

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