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Article

An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13.

Human molecular genetics - 1 Sept 1993

Dittrich B, Gross S, Buiting K, Horsthemke B

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Share to Alleles
Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 15
Share to Deoxyribonucleases, Type II Site-Specific

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Restriction Fragment Length

Share to Prader-Willi Syndrome

Source

Identifiers

PMID: 7902166
DOI: 10.1093/hmg/2.9.1509

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13.PMID 7902166Read ↗

An insertion/deletion polymorphism at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13.Semantic proximity Read ↗

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.Semantic proximity Read ↗

A DraI RFLP detected for probe pIR4-3R [D15S11] on chromosome 15q.Semantic proximity Read ↗

Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndromeSemantic proximity Read ↗

Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15.Semantic proximity Read ↗

Imprinting-mutation mechanisms in Prader-Willi syndrome.Semantic proximity Read ↗

Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13.Semantic proximity Read ↗

A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype.Semantic proximity Read ↗

The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection.Semantic proximity Read ↗

A 28-kb deletion spanning D15S63 (PW71) in five families: a rare neutral variant?Semantic proximity Read ↗

MspI RFLP at 19q13.3 identified by the anonymous DNA sequence pX75B (D19S112).Semantic proximity Read ↗

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.Semantic proximity Read ↗

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