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

An unreported RFLP for probe 218 EP6 that is useful in linkage analysis of adult polycystic kidney disease.

Human genetics - 1 Oct 1993

Jeffery S, Morgan S

Abstract excerpt

Probe 218 EP6 is known to recognise two restriction fragment length polymorphisms (RFLPs) after digestion of genomic DNA with PvuII. We report a rare allele that segregates in Mendelian fashion, in a family where adult polycystic kidney disease was being tracked using linked polymorphisms.

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chromosomes, Human, Pair 16
Share to DNA

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA Probes

Share to Genetic Linkage

Share to Pedigree

Share to Polymorphism, Genetic

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 7901145
DOI: 10.1007/BF01247352

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

An unreported RFLP for probe 218 EP6 that is useful in linkage analysis of adult polycystic kidney disease.PMID 7901145Read ↗

An RFLP for probe 26-6 that is useful in linkage diagnosis for adult polycystic kidney disease.Semantic proximity Read ↗

Probe 87-10a identifies a codominantly inherited X chromosome allele polymorphic in three racial populations.Semantic proximity Read ↗

A single genetic locus for adult polycystic kidney disease in five Australian families of southern European origin.Semantic proximity Read ↗

Adult polycystic kidney disease in a kindred of West Indian origin exhibits linkage with the 3'HVR probe on chromosome 16.Semantic proximity Read ↗

A novel mutation identified in PKHD1 by targeted exome sequencing: guiding prenatal diagnosis for an ARPKD family.Semantic proximity Read ↗

Detection of a novel nonsense mutation and an intragenic polymorphism in the PKD1 gene of a Cypriot family with autosomal dominant polycystic kidney disease.Semantic proximity Read ↗

Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.Semantic proximity Read ↗

A new polymorphic probe on chromosome 22q (XD6) (D22S313).Semantic proximity Read ↗

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