Polymorphic Markers for the Arylsulfatase A Gene Reveal a Greatly Expanded Meiotic Map for the Human 22q Telomeric Region-Reference-Cited by-同舟云学术

Polymorphic Markers for the Arylsulfatase A Gene Reveal a Greatly Expanded Meiotic Map for the Human 22q Telomeric Region

Published:2000-02 Issue:3 Volume:63 Page:430-432
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Brennan Mark D.,Neibergs Holly L.,Phillips Kay,Moseley Steve

Publisher

Elsevier BV

Subject

Genetics

Reference9 articles.

1. Coincidence of two novel arylsulfatase A alleles and mutation 459+1G>A within a family with metachromatic leukodystrophy: Molecular basis of phenotypic heterogeneity;Berger;Hum. Mutat.,1999

2. A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination;Blouin;Am. J. Hum. Genet.,1995

3. Comprehensive human genetic maps: Individual and sex-specific variation in recombination;Broman;Am. J. Hum. Genet.,1998

4. Cox-Matise, T, Perlin, M, and, Chakravarti, A. 1996, MultiMap, Automated genetic linkage mapping, version 2.0.

5. A comprehensive genetic map of the human genome based on 5,264 microsatellites;Dib;Nature,1996

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1. Evidence for two schizophrenia susceptibility genes on chromosome 22q13;Psychiatric Genetics;2007-10

2. Transmission disequilibrium suggests a role for the sulfotransferase-4A1 gene in schizophrenia;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2005

3. Infantile metachromatic leukodystrophy (MLD) in a compound heterozygote for the c.459 + 1G > A mutation and a complete deletion of theARSA gene;American Journal of Medical Genetics;2004

4. Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations;Journal of Medical Genetics;2003-09-01

5. Sequence diversity ofKIAA0027/MLC1:are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?;Human Mutation;2002-12-20