Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy-Reference-Cited by-同舟云学术

Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy

Published:1998-07 Issue:1 Volume:63 Page:181-190
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Cacurri S.,Piazzo N.,Deidda G.,Vigneti E.,Galluzzi G.,Colantoni L.,Merico B.,Ricci E.,Felicetti L.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. The FSH-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter;Bakker;Muscle Nerve Suppl,1995

2. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD);Cacurri;Hum Genet,1994

3. Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the FSHD locus on chromosome 4qter;Deidda;Eur J Hum Genet,1995

4. 4q35 Molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy;Deidda;Ann Neurol,1994

5. Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD);Deidda;J Med Genet,1996

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