Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genealogical study of myotonic dystrophy in Istria (Croatia).

Annales de genetique - 1 Jan 2000

Medica I, Logar N, Mileta D Leonardelli, Peterlin B

Abstract excerpt

High prevalence of myotonic dystrophy (DM) of 18.1 per 100,000 has been found in Croatian region Istria, a region where a great mixture of nations occurred over the last three centuries. The objective of this study was to test the hypothesis of common ancestry in Istrian DM families. Pedigrees were constructed on the basis of extensive family history obtained from the patients in all Istrian DM families. Church...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Croatia
Share to Genetic Markers
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetics, Population

Share to Myotonic Dystrophy

Share to Pedigree

Source

Identifiers

PMID: 15183746
DOI: 10.1016/j.anngen.2003.08.026

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genealogical study of myotonic dystrophy in Istria (Croatia).PMID 15183746Read ↗

Characteristics of myotonic dystrophy in Istria: molecular genetics approach--mutation analysis.Semantic proximity Read ↗

Croatian genetic heritage: an updated Y-chromosome story.Semantic proximity Read ↗

Reconstructing the Indian origin and dispersal of the European Roma: a maternal genetic perspective.Semantic proximity Read ↗

Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.Semantic proximity Read ↗

Mendelian diseases among Roman Jews: implications for the origins of disease alleles.Semantic proximity Read ↗

Haplotype analysis of genomic polymorphisms in and around the myotonic dystrophy locus in diverse populations of India.Semantic proximity Read ↗

Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis.Semantic proximity Read ↗

A genetic profile of Romany (Gypsy) subethnic group from a single region in Slovakia.Semantic proximity Read ↗

CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia.Semantic proximity Read ↗

Molecular anatomy of CTG expansion in myotonin protein kinase gene among myotonic dystrophy patients from eastern India.Semantic proximity Read ↗

A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia.Semantic proximity Read ↗

Y chromosomal heritage of Croatian population and its island isolates.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.