Contiguous deletion syndromes
References and recommended reading (32)
Contiguous Gene Syndromes: a Component of Recognizable Syndromes
J Pediatr
(1986)- et al.
Two Families of Low-Copy Number Repeats are Interspersed on Xp22.3: Implications for the High Frequency of Deletions in This Region
Genomics
(1990) - et al.
An Xp22 Microdeletion Associated with Ocular Albinism and Ichthyosis: Approximation of Breakpoints and Estimation of Deletion Size by Using Cloned DNA Probes and Flow Cytometry
Am J Hum Genet
(1989) - et al.
Isolation and Characterization of a Zinc-Finger Polypeptide Gene at the Human Chromosome 11 Wilms' Tumor Locus
Cell
(1990) - et al.
Wilms' Tumor Locus on 11p13 Defined by Multiple CpG Island-Associated Transcripts
Science
(1990) - et al.
Cloning of Defined Regions of the Human Genome by Microdissection of Banded Chromosomes and Enzymatic Amplification
Nature
(1989) Microdeletions and Mendelian Phenotypes
Molecular Cytogenetics: Toward Dissection of the Contiguous Gene Syndromes
Am J Hum Genet
(1988)- et al.
Molecular Cytogenetics: Interlace of Cytogenetics and Monogenic Disorders
Disorders of Glycerol Metabolism
Minor Xp21 Chromosome Deletion in a Male Associated with Expression of Duchenne Muscular Dystrophy, Chronic Granulomatous Disease, Retinitis Pigmentosa and McLeod Syndrome
Am J Hum Genet
(1985)
Isolation of Candidate cDNAs for Portions of the Duchenne Muscular Dystrophy Gene
Nature
(1986)
Cloning the Gene for an Inherited Human Disorder-Chronic Granulomatous Disease—on the Basis of its Chromosomal Localization
Nature
(1986)
Deletion Mapping of Aland Island Eye Disease Xp21 Between DXS67 (B24) and Duchenne Muscular Dystrophy
Am J Hum Genet
(1990)
Localization of the Aland Island Eye Disease Locus to the Percientromeric Region of the X Chromosome by Linkage Analysis
Am J Hum Genet
(1990)
X-linked Ichthyosis due to Steroid Sulphatase Deficiency Associated with Kallmann Syndrome (Hypogonadotropic Hypogonadism and Anosmia): Linkage Relationships with Xg and Cloned DNA Sequences from The Distal Short Arm of the X Chromosome
Hum Genet
(1986)
Cited by (25)
Overlap of autism spectrum disorder and glucose transporter 1 deficiency syndrome associated with a heterozygous deletion at the 1p34.2 region
2015, Journal of the Neurological SciencesA chromosomal deletion map of human malformations
1998, American Journal of Human GeneticsThe human genetic map
1992, Current Opinion in BiotechnologyTracking disease genes by reverse genetics
1992, Journal of Psychiatric Research
Copyright © 1991 Published by Elsevier Ltd.