Literature DB >> 2443701

Molecular genetics of human chromosome 16.

G R Sutherland1, S Reeders, V J Hyland, D F Callen, A Fratini, J C Mulley.   

Abstract

The major diseases mapped to chromosome 16 are adult polycystic kidney disease and those resulting from mutations in the alpha globin complex. There are at least six other less important genetic diseases which map to this chromosome. The adenine phosphoribosyltransferase gene allows for selection of chromosome 16 in somatic cell hybrids and a hybrid panel is available which segments the chromosome into six regions to facilitate gene mapping. Genes which have been mapped to this chromosome or which have had their location redefined since HGM8 include APRT, TAT, MT, HBA, PKD1, CTRB, PGP, HAGH, HP, PKCB, and at least 19 cloned DNA sequences. There are RFLPs at 13 loci which have been regionally mapped and can be used for linkage studies.

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Year:  1987        PMID: 2443701      PMCID: PMC1050200          DOI: 10.1136/jmg.24.8.451

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


  19 in total

1.  Isolation and sequence of a rat chymotrypsin B gene.

Authors:  G I Bell; C Quinto; M Quiroga; P Valenzuela; C S Craik; W J Rutter
Journal:  J Biol Chem       Date:  1984-11-25       Impact factor: 5.157

Review 2.  Alpha-thalassemia.

Authors:  D R Higgs; D J Weatherall
Journal:  Curr Top Hematol       Date:  1983

3.  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

4.  New regional localisations for HAGH and PGP on human chromosome 16.

Authors:  J C Mulley; D F Callen
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

5.  The haemoglobin H disease mental retardation syndrome: molecular studies on the South African case.

Authors:  A M Bowcock; S van Tonder; T Jenkins
Journal:  Br J Haematol       Date:  1984-01       Impact factor: 6.998

6.  Human metallothionein genes are clustered on chromosome 16.

Authors:  M Karin; R L Eddy; W M Henry; L L Haley; M G Byers; T B Shows
Journal:  Proc Natl Acad Sci U S A       Date:  1984-09       Impact factor: 11.205

7.  The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes.

Authors:  A E Felice; M P Cleek; K McKie; V McKie; T H Huisman
Journal:  Blood       Date:  1984-05       Impact factor: 22.113

8.  Hemoglobin H disease and multiple congenital anomalies in a child of northern European origin.

Authors:  B Hjelle; S Charache; J A Phillips
Journal:  Am J Hematol       Date:  1982-12       Impact factor: 10.047

9.  Localization of the haptoglobin alpha and beta genes (HPA and HPB) to human chromosome 16q22 by in situ hybridization.

Authors:  J R McGill; F Yang; W D Baldwin; J L Brune; D R Barnett; B H Bowman; C M Moore
Journal:  Cytogenet Cell Genet       Date:  1984

10.  Metallothionein gene cluster is split by chromosome 16 rearrangements in myelomonocytic leukaemia.

Authors:  M M Le Beau; M O Diaz; M Karin; J D Rowley
Journal:  Nature       Date:  1985 Feb 21-27       Impact factor: 49.962

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  3 in total

1.  A linkage group with FRA16B (the fragile site at 16q22.1).

Authors:  J C Mulley; V J Hyland; A Fratini; L J Bates; A K Gedeon; G R Sutherland
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

2.  Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.

Authors:  V J Hyland; S Grist; D F Callen; G R Sutherland
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

3.  Adult polycystic kidney disease.

Authors:  R Harris
Journal:  J Med Genet       Date:  1987-08       Impact factor: 6.318

  3 in total

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