A Genĉík

Health needs of the Roma population in the Czech and Slovak Republics

Origins and Divergence of the Roma (Gypsies)

Incidence in Sweden and Clinical Features of Familial Hemophagocytic Lymphohistiocytosis

Hoxb2 and Hoxb4 Act Together to Specify Ventral Body Wall Formation

Identification of factors associated with high breast cancer risk in the mothers of children with soft tissue sarcoma.

Genetic studies of the Roma (Gypsies): a review

Head and neck cancer

HLH‐2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis

Laryngeal carcinoma in a lynch syndrome II kindred

FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS

Role of Genetic Factors in the Etiology of Squamous Cell Carcinoma of the Head and Neck

Hereditary Colorectal Cancer

Induction of apoptosis and caspase activation in cells obtained from familial haemophagocytic lymphohistiocytosis patients

Familial Hemophagocytic Lymphohistiocytosis: Clinical Review Based on the Findings in Seven Children

Head and Neck Cancer

Familial hemophagocytic lymphohistiocytosis and viral infections

Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer

Cytochrome P450 enzymes in drug metabolism: Regulation of gene expression, enzyme activities, and impact of genetic variation

Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Role of CYP1B1 in Glaucoma

Chromosome 3p deletions in head and neck carcinomas: Statistical ascertainment of allelic loss

Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members

Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms

5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

Recurrence of diaphragmatic agenesis associated with multiple midline defects: Evidence for an autosomal gene regulating the midline

Hypercytokinemia in familial hemophagocytic lymphohistiocytosis

Hematological Problems in Pediatric Intensive Care

Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal-recessive inheritance and complete penetrance.

Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect

Genetic heterogeneity of congenital glaucoma

Familial and histological analyses of 138 breast cancer patients

Familial occurrence of congenital diaphragmatic defect in three families.

Genetic analysis of familial erythrophagocytic lymphohistiocytosis

High Incidence of Laryngeal Carcinoma in a Swiss Family