Linkage analysis of maturity-onset diabetes of the young (MODY): genetic heterogeneity and nonpenetrance.
Explore this paper's citation graph
Summary
Analysis strongly suggests that MODY as expressed in the EDI and WIS families is unlinked to loci on chromosome 20, and three polymorphic loci-D20S16, D20S17, and ADA--show no recombination with the MODY locus when two-point linkage analysis is used in the early-onset branches of the family.
- Type
- article
- Published
- 1992-03-01
- Cited by
- 27
- References
- 11
- Access
- Open access
- OpenAlex
- https://openalex.org/W304086187
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:33886953
Keywords
Genetics, Genetic linkage, Locus (genetics), Allele, Biology
References
- Identification of more than 500 RFLPs by screening random genomic clones.
- Analysis of Human Genetic Linkage
- Strategies for multilocus linkage analysis in humans.
- A genetic linkage map of 32 loci on human chromosome 10.
- Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
- The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome.
- A genetic linkage map of the human genome.
- The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.
- MODY: a model for the study of the molecular genetics of NIDDM.
Cited by
- Analysis of the glucokinase gene in Mexican families displaying early-onset non-insulin-dependent diabetes mellitus including MODY families.
- The Human Genome Project and eugenic concerns.
- Exclusion of adenosine deaminase gene locus on chromosome 20q12–13.1 in familial NIDDM in Taiwanese patients
- New Susceptibility Locus for NIDDM Is Localized to Human Chromosome 20q
- D20S16 is a complex interspersed repeated sequence: genetic and physical analysis of the locus.
- Molecular genetics of diabetes mellitus.
- Availability of Type II Diabetic Families for Detection of Diabetes Susceptibility Genes
- Physical localization of chromosome 20 markers using somatic cell hybrid cell lines and fluorescence in situ hybridization.
- Molecular studies of the genetics of non–insulin‐dependent diabetes mellitus
- Screening for NIDDM: Opportunities for detection, treatment, and prevention
- Linkage and molecular scanning analyses of MODY3/hepatocyte nuclear factor-1 alpha gene in typical familial type 2 diabetes: evidence for novel mutations in exons 8 and 10.
- Type 2 diabetes mellitus in children.
- Early-onset type-ll diabetes mellitus (MODY4) linked to IPF1
- Genetic and environmental determinants of non-insulin-dependent diabetes mellitus (NIDDM).
- Type II Diabetes: Clinical Aspects of Molecular Biological Studies
- A microsatellite polymorphism associated with the PLC1 (phospholipase C) locus: identification, mapping, and linkage to the MODY locus on chromosome 20.
- Association of Pulmonary Surfactant Protein A (SP-A) Gene and Respiratory Distress Syndrome: Interaction with SP-B
- Genetic initiation of hypertensive and diabetic nephropathy.
- Linkage of Genetic Markers on Human Chromosomes 20 and 12 to NIDDM in Caucasian Sib Pairs With a History of Diabetic Nephropathy
- Genetic and Genomic Discovery Using Family Studies
Related papers
- Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54).
- Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan
- Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21.
- A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.
- Genetic heterogeneity in families with hereditary multiple exostoses.
- Susceptibility genes for familial Alzheimer's disease on chromosomes 19 and 21: A reality check
- Genetic heterogeneity and Alzheimer`s disease
- Examination of candidate chromosomal regions for type 2 diabetes reveals a susceptibility locus on human chromosome 8p23.1.
- Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2