Literature DB >> 5611035

Ring D chromosome: a second case associated with anomalous haptoglobin inheritance.

G E Bloom, P S Gerald, L E Reisman.   

Abstract

A second child with a ring D chromosome and anomalous inheritance of haptoglobin has been identified. Autoradiographic studies of peripheral lymphocytes from this child and of those from the previously described patient indicate that the ring in each is derived from chromosome No. 13. These findings are evidence that the locus for the haptoglobin alpha-chain is situated on one end of chromosome No. 13.

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Year:  1967        PMID： 5611035     DOI： 10.1126/science.156.3783.1746

Source DB:  PubMed          Journal:  Science        ISSN： 0036-8075            Impact factor:   47.728


  12 in total

1.  Chromosome banding patterns in an infant with 13q minus syndrome.

Authors:  T Ikeuchi; S Sonta; M Sasaki; M Hujita; K Tsunematsu
Journal:  Humangenetik       Date:  1974-03-28

Review 2.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

3.  Ring 13 chromosome with normal haptoglobin inheritance.

Authors:  J G Hollowell; L G Littlefield; A Dharmkrong-AT; G M Folger; C W Heath; G E Bloom
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

4.  The 13q- deletion syndrome.

Authors:  E Grace; J Drennan; D Colver; R R Gordon
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

5.  The 13q-deletion syndrome.

Authors:  P W Allderdice; J G Davis; O J Miller; H P Klinger; D Warburton; D A Miller; F H Allen; C A Abrams; E McGilvray
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

6.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

7.  Localization of genes on chromosome 13: analysis of two kindreds.

Authors:  G E Bloom; P S Gerald
Journal:  Am J Hum Genet       Date:  1968-11       Impact factor: 11.025

8.  Dq-, Dr and retinoblastoma.

Authors:  A I Taylor
Journal:  Humangenetik       Date:  1970

9.  Absent IgA and deletions of chromosome 18.

Authors:  J M Stewart; S Go; E Ellis; A Robinson
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

10.  D1 ring chromosome in newborn with peculiar face, polydactyly, imperforate anus, arrhinencephaly, and other malformations.

Authors:  A R Biles; T Lüers; K Sperling
Journal:  J Med Genet       Date:  1970-12       Impact factor: 6.318
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