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Literature DB >> 6978612

Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4.

R E Ferrell, H M Hittner, F L Kretzer, J H Antoszyk.

Abstract

Thirty-seven blood samples were analyzed for linkage from members of a single family with an anterior segment mesenchymal dysgenesis (ASMD1) with variable expressivity affecting members of at least six generations. Maximum-likelihood analysis for linkage between ASMD1 and 14 biochemical and serological markers in the family showed a probable linkage between ASMD1 and the MNS blood group on the long arm of chromosome 4 (Z = 2.36 at a recombination fraction of .09).

Entities: Disease

Mesh：

Substances：

Year: 1982 PMID： 6978612 PMCID： PMC1685280

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

11 in total

1. Genetic polymorphism of human phosphoglycolate phosphatase (PGP).

Authors: R F Barker; D A Hopkinson
Journal: Ann Hum Genet Date: 1978-10 Impact factor: 1.670

2. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors: J Ott
Journal: Am J Hum Genet Date: 1974-09 Impact factor: 11.025

Review 3. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5.

Authors: D Bootsma; P J McAlpine
Journal: Cytogenet Cell Genet Date: 1979

4. Further studies of congenital hereditary endothelial dystrophy of the cornea.

Authors: K R Kenyon; A E Maumenee
Journal: Am J Ophthalmol Date: 1973-10 Impact factor: 5.258

5. Congenital corneal leukomas. 1. Central defect in Descemet's membrane.

Authors: W M Townsend
Journal: Am J Ophthalmol Date: 1974-01 Impact factor: 5.258

6. Analysis of crossingover in man.

Authors: N E Morton
Journal: Cytogenet Cell Genet Date: 1978

7. Group-specific component: evidence for two subtypes of the Gc1 gene.

Authors: J Constans; M Viau
Journal: Science Date: 1977-12-09 Impact factor: 47.728

8. The Multinational Andean Genetic and Health Program. IX. Gene frequencies and rare variants of 20 serum proteins and erythrocyte enzymes in the Aymara of Chile.

Authors: R E Ferrell; T Bertin; S A Barton; F Rothhammer; W J Schull
Journal: Am J Hum Genet Date: 1980-01 Impact factor: 11.025

Anterior segment mesenchymal dysgenesis: probable linkage to the MNS blood group on chromosome 4.

1. Genetic polymorphism of human phosphoglycolate phosphatase (PGP).

2. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Review 3. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5.

4. Further studies of congenital hereditary endothelial dystrophy of the cornea.

5. Congenital corneal leukomas. 1. Central defect in Descemet's membrane.

6. Analysis of crossingover in man.

7. Group-specific component: evidence for two subtypes of the Gc1 gene.

8. The Multinational Andean Genetic and Health Program. IX. Gene frequencies and rare variants of 20 serum proteins and erythrocyte enzymes in the Aymara of Chile.

9. Anterior chamber cleavage syndrome. A stepladder classification.

10. Variable expressivity of autosomal dominant anterior segment mesenchymal dysgenesis in six generations.

1. Pairwise linkage analysis of 11 loci on human chromosome 4.

2. Atypical vitelliform macular dystrophy in a 5-generation family.

3. The mouse Cat4 locus maps to chromosome 8 and mutants express lens-corneal adhesion.