016 : Aguirre Samudio et al : Polymorphism of the exon 3, DRD4 gene, in patients with the first psychotic episode 017 : Al-Gazali et al : Further Delineation of Hennekam Syndrome 018 : Albertini et al : The German National Genome Research Network NGFN - A New Interdisciplinary Approach to Systematically Explore the Genetic Basis of Complex Diseases 019 : Barajas-Barajas et al : Sensorineural Deafness in two infants: a novel feature in the 22q distal duplication syndrome 020 : Ruiz-Cruz et al : Loss of expression of H19 gene in Beckwith-Wiedemann and Wilms tumor Mexican Children 021 : Berdón-Zapata et al : p63 Gene Analysis in Subjects with Syndromic and Isolated Ectrodactyly 023 : Cabrera Vázquez et al : Study of the genes IPF1, TCF1 and Glucocinasa in Mexican Women with Gestacional Diabetes 024 : Camarena et al : Positive family-based association between MAO-A gene and obesity 025 : Canizales-Quinteros et al : A Mexican kindred with familial hypercholesterolemia linked to chromosome 1p32 026 : Cheah et al : Age-dependent association of the Trp2 allele of the COL9A2 gene with intervertebral disc degeneration in Southern Chinese 027 : Cornejo-Roldán et al : One year experience using qualitative metabolic screening in pediatrician patients 028 : Cortes-Gutierrez et al : Evaluation of sex chromosome aneuploidies in patients with Turner syndrome by G-banding and FISH techniques: A serial case study 029 : D'Urso et al : Distal Xq28 region: Analysis of two peculiar cases of Incontinentia Pigmenti (IP) and search for new genetic markers 030 : David et al : Molecular characterization of a familial translocation implicates HDAC9 and TGFB2 in the pathogenesis of Peters' anomaly 031 : Diaz-Anzaldua et al : Association between 7q31 markers and Tourette Syndrome 032 : Dávalos et al : Clinical Analysis in Patients of Gorlin Syndrome in North-West of Mexico 033 : Dávalos-Rodríguez et al : Kabuki Syndrome: First familial case in Mexico and review of the literature 034 : Ewald et al : A genomewide search for chromosome segment or haplotype sharing among patients with bipolar affective disorder from the Faroe Islands 035 : Fernandez-Novoa et al : ACE I/D polymorphism-related phenotypic variation in dementia 036 : Figuera et al : Frontometaphyseal Dysplasia: Presentation of severe form in a female 037 : Fuchs et al : Quality control and problem analysis in molecular diagnostic laboratories 038 : Fukumaki et al : Association Studies of Schizophrenia with Evenly Distributed SNPs in the Metabotropic Glutamate Receptor Gene Regions 040 : Galimberti et al : Quantitative molecular monitoring of minimal residual disease in follicular lymphoma patients treated by anti-CD20 antibody and high-dose therapy: efficacy of Rituximab as in vivo purging tool 041 : Garcia-Ubbelohde et al : A novel technique to support neonatal screening for congenital hypothyroidism 043 : Glavac : Mutations in Type IV Collagen Chains (COL4A3, COL4A4 and COL4A5) in Relation to Alport Syndrome and Familial Hematuria 044 : Gonzalez-Herrera et al : Common polymorphisms in the MTHFR and CBS folate genes are not associated risk factors for neural tube defects in the State of Yucatan, Mexico 045 : Guo et al : A Large-Scale Transcriptional Profiling of Endometriotic Lesions 046 : Herrera-Nájera et al : Frequency of polymorphisms C677T and A1298C in MTHFR gene and 844ins68 bp in CBS gene in association with preeclamsia/eclampsia in Mexican women 047 : Huertas-Vázquez et al : Replication of Linkage to Chromosome 1q21q23 in Familial Combined Hyperlipidemia Mexican Families 048 : Ibarra et al : Molecular spectrum of Beta thalassemia in Mexican Population 049 : Jaloma Cruz et al : PCR detection of factor VIII inversion in Mexican families with severe haemophilia A 050 : Jimenez-Sanchez et al : Human disease genes: Protein function and clinical phenotypes 051 : Kucinskas et al : Nine novel COL1A1 gene mutations in Lithuanian patients with osteogenesis imperfecta 052 : López et al : MTHFR C677T and MTRR A66G gene mutations, folates and vitamin B12 intake and neural tube defects in a sample of the Mexican population 053 : MacDonald et al : Genome-wide detection of segmental duplications and assembly errors in the human genome sequence 054 : Macías Gómez et al : Relation of the rearrangements in the gamma and delta genes of the TCR, with the prognosis of ALL-B patients 055 : Mantilla et al : Intron 13 microsatellite of factor VIII gene in Mexican population and its application for haemophilia A carrier diagnosis 056 : Molina et al : CFTR gene mutations in Chilean Cystic Fibrosis and Chronic Rhinosinusitis patients 057 : Moran et al : Chromosome 13q partial duplication. Report of a Mexican case 058 : Mutchinick et al : Prevalence of the C282Y and H63D mutations of the HFE gene in a sample of patients with hereditary hemochromatosis, healthy mestizos and two Indian groups from the State of Chiapas 059 : Nińo de Rivera et al : Clinic, Genetic and Molecular Study of Primary Open Angle Glaucoma in Mexico 060 : Nosikov et al : Antioxidant Scavenging and Peroxide Inactivating Enzyme Genes Involved in the Genetic Susceptibility to Ischemic Heart Disease 062 : Prokunina et al : Finding genes for complex diseases in complex populations: the case of Systemic Lupus Erythematosus (SLE) 063 : Ramos et al : Abnormal localization of the sequence D13Z1/D21Z1 on the centromeric 22 region in a father of a trisomic 21 child 064 : Rascón Sabido et al : Neurofibromatosis type I associated with Amyotrophic Lateral Sclerosis: Case Report 065 : Rasmussen et al : Low Frequency of Friedreich Ataxia in the Mexican Mestizo population 066 : Ruiz-Portillo et al : Association among homocysteine gene polymorphisms (C677T, A1298C in MTHFR and 844ins68 in CBS) with atheroesclerotic cardiovascular disease in Mexican patients 067 : Sanchez et al : Aneuploidy for chromosomes X, Y, 18 and 21 in sperm from Hodgkin's disease patients treated before and after puberty with nitrogen Mustard, Oncovin, Procarbazine and Prednisone (MOPP) chemotherapy 068 : Scardovi et al : Automated transcript mapping detects brain-specific gene isoforms in a region on 16p13 associated with autism 069 : Shadrina et al : Molecular genetic analysis of sporadic amyotrophic lateral sclerosis patients from Russia 070 : Shen et al : Association study of SNP combination pattern in dopaminergic pathway with paranoid schizophrenia - A novel strategy for complex disorder 071 : Skaug et al : The Centre for Applied Genomics at Toronto's Hospital for Sick Children, Canada 072 : Smith et al : Genomic Instability and Schizophrenia 073 : Toda et al : Genome-wide microsatellite association studies for Parkinson's disease by using the pooled DNA method 074 : Wong-Ley et al : Development of a diagnostic program for muscular dystrophies 075 : Yescas Gómez et al : A founder mutation in Presenilin 1 causing early onset Alzheimer disease in unrelated Mexican families 076 : Zatz et al : MAOA polymorphism and alcoholism in males as compared to females 077 : Zepeda Romero et al : Gorlin syndrome: Report of a Mexican family with emphasis on ocular features 078 : Zhong et al : Identification of FMRP-binding RNAs: A novel approach searching for in vivo protein-RNA interactions 079 : Zielenski et al : Haplotype analysis of CFM1 region in human chromosome 19q13 associated with meconium ileus in patients with cystic fibrosis 080 : Zúńiga et al : Distribution of polymorphisms in ccr5 and HLA B genes in HIV-infected Mexican Mestizo and in HIV seronegative Mexican Mestizo and Amerindian individuals: implications for the natural history of HIV infection in Mexico
AbProcess V2.10 - Written by Alastair Brown
Copyright (C) 1999-2003 Alastair Brown