Andre Reis
0000-0002-6301-6363
279 papers found
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Palmoplantar Keratoderma in Association with Carcinoma of the Esophagus Maps to Chromosome 17q Distal to the Keratin Gene Cluster
Fructose-1,6-Bisphosphatase: Genetic and Physical Mapping to Human Chromosome 9q22.3 and Evaluation in Non-Insulin-Dependent Diabetes Mellitus
No Evidence for Segregation Distortion of Cystic-Fibrosis Alleles Among Sibs of Cystic-Fibrosis Patients
Recurrent nasal polyps as a monosymptomatic form of cystic fibrosis associated with a novel in-frame deletion (591del18) in the CFTR gene
The Ataxia-Telangiectasia-Variant Gene-1 and Gene-2 Are Distinct From the Ataxia-Telangiectasia Gene on Chromosome-11q23.1
Epidermolytic Palmoplantar Keratoderma of Vorner - Clinical-Features, Formal Genetics, and Molecular Biological Findings in 22 Families
Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster
Pancreatic insufficiency and pulmonary disease in German and Slavic cystic fibrosis patients with the R347P mutation
The critical region for Angelman syndrome lies between D15S122 and D15S113
A YAC Contig Spanning the Nevoid Basal Cell Carcinoma Syndrome, Fanconi Anaemia Group C, and Xeroderma Pigmentosum Group A Loci on Chromosome 9q
Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma
The origin of the major cystic fibrosis mutation (ΔF508) in European populations
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)
Population variation of common cystic fibrosis mutations. The Cystic Fibrosis Genetic Analysis Consortium
Trinucleotide repeat polymorphism at the PKLR locus
Mutations in the Pyruvate-Kinase-L Gene in Patients With Hereditary Hemolytic-Anemia
Linkage analysis in German breast cancer families with early onset of the disease, using highly polymorphic markers from the chromosome 17q11-q24 region.
Environmental Trichlorfon and Cluster of Congenital Abnormalities:
Dinucleotide repeat polymorphism at the locus D13S231
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