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Literature DB >> 3669048

Exclusion mapping.

Abstract

The basis for using information against linkage to some loci to support linkage to other loci is discussed and data on cystic fibrosis available up to late July 1985 used as an example.

Entities: Disease

Mesh：

Year: 1987 PMID： 3669048 PMCID： PMC1050264 DOI： 10.1136/jmg.24.9.539

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

9 in total

1. Sequential tests for the detection of linkage.

Authors: N E MORTON
Journal: Am J Hum Genet Date: 1955-09 Impact factor: 11.025

2. A search for linkage in cystic fibrosis.

Authors: M C Goodchild; J H Edwards; K P Glenn; C Grindey; R Harris; P Mackintosh; J Wentzel
Journal: J Med Genet Date: 1976-12 Impact factor: 6.318

3. The analysis of X-linkage.

Authors: J H Edwards
Journal: Ann Hum Genet Date: 1971-02 Impact factor: 1.670

4. A meiotic linkage map of the human male.

Authors: J H Edwards; J Parekh; V Kirton; M Hultén
Journal: Cytogenet Cell Genet Date: 1978

5. Exclusion mapping illustrated by the MNSs blood group.

Authors: P J Cook; J E Noades; C G Lomas; K E Buckton; E B Robson
Journal: Ann Hum Genet Date: 1980-07 Impact factor: 1.670

6. Data and theory for a revised chiasma map of man.

Authors: N E Morton; J Lindsten; L Iselius; S Yee
Journal: Hum Genet Date: 1982 Impact factor: 4.132

7. Interpretation of LOD scores with a set of marker loci.

Authors: E A Thompson
Journal: Genet Epidemiol Date: 1984 Impact factor: 2.135

Review 8. Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors: D Botstein; R L White; M Skolnick; R W Davis
Journal: Am J Hum Genet Date: 1980-05 Impact factor: 11.025

9. Linkage relationships of paraoxonase (PON) with other markers: indication of PON-cystic fibrosis synteny.

Authors: H Eiberg; J Mohr; K Schmiegelow; L S Nielsen; R Williamson
Journal: Clin Genet Date: 1985-10 Impact factor: 4.438

9 in total

19 in total

Exclusion mapping.

1. Sequential tests for the detection of linkage.

2. A search for linkage in cystic fibrosis.

3. The analysis of X-linkage.

4. A meiotic linkage map of the human male.

5. Exclusion mapping illustrated by the MNSs blood group.

6. Data and theory for a revised chiasma map of man.

7. Interpretation of LOD scores with a set of marker loci.

Review 8. Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

9. Linkage relationships of paraoxonase (PON) with other markers: indication of PON-cystic fibrosis synteny.

1. Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.

2. A genetic study of the human low-voltage electroencephalogram.

3. The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.

4. An exclusion map for pre-eclampsia: assuming autosomal recessive inheritance.

5. Exclusion map of Salla disease: attempts to localize the disease gene using a computer program.

6. Reply to "The question of heterogeneity in Marfan syndrome"

7. An exclusion map of Marfan syndrome.

8. The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6.

9. Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family.

10. Exclusion of familial dysautonomia from more than 60% of the genome.