Literature DB >> 2997740

An anonymous single copy chromosome 22 clone, D22S10 (22c1-18) identifies an RFLP with PstI.

M H Hofker, M H Breuning, E Bakker, G J van Ommen, P L Pearson.   

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Year:  1985        PMID： 2997740      PMCID： PMC322031          DOI： 10.1093/nar/13.19.7167

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  7 in total

1.  Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome.

Authors:  A M Sharkey; L McLaren; M Carroll; J Fantes; D Green; D Wilson; P J Scambler; H J Evans
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Authors:  G A Rouleau; B R Seizinger; W Wertelecki; J L Haines; D W Superneau; R L Martuza; J F Gusella
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

3.  Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis.

Authors:  C G Mathew; K Thorpe; D F Easton; C Carter; C Wallis; Z Wong; A J Jeffreys; B A Ponder
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

Review 4.  Human chromosome 22.

Authors:  J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal:  J Med Genet       Date:  1987-02       Impact factor: 6.318

5.  Loss of heterozygosity and the origin of meningioma.

Authors:  E Meese; N Blin; K D Zang
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

6.  Comparative mapping of the constitutional and tumor-associated 11;22 translocations.

Authors:  M Budarf; B Sellinger; C Griffin; B S Emanuel
Journal:  Am J Hum Genet       Date:  1989-07       Impact factor: 11.025

7.  Deletion mapping of chromosome 1p and 22q in pheochromocytoma.

Authors:  E Shin; S Fujita; K Takami; H Kurahashi; Y Kurita; T Kobayashi; T Mori; I Nishisho; S Takai
Journal:  Jpn J Cancer Res       Date:  1993-04
  7 in total

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