Literature DB >> 2448751

Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 [D10S15].

Y Nakamura1, M Carlson, K Krapcho, J Gill, P O'Connell, M Leppert, G M Lathrop, J M Lalouel, R White.   

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Year:  1988        PMID： 2448751      PMCID： PMC334655          DOI： 10.1093/nar/16.1.374

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


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  5 in total

1.  Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors:  Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal:  Science       Date:  1987-03-27       Impact factor: 47.728

2.  Report of the Committee on the Genetic Constitution of Chromosomes 10, 11, and 12.

Authors:  K H Grzeschik; H H Kazazian
Journal:  Cytogenet Cell Genet       Date:  1985

3.  A single copy subclone, p1-101, from cosmid 3-3B, defines three RFLPs on 10pter-q23 [HGM9 no. D10S4].

Authors:  M Litt; O T Mueller; T B Shows; R Litt
Journal:  Nucleic Acids Res       Date:  1987-03-25       Impact factor: 16.971

4.  Bgl II RFLP recognized by a human IRBP cDNA localized to chromosome 10.

Authors:  G I Liou; Y Li; C Wang; S L Fong; S Bhattacharya; C D Bridges
Journal:  Nucleic Acids Res       Date:  1987-04-10       Impact factor: 16.971

5.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025
  5 in total
  7 in total

1.  Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma.

Authors:  S A Narod; H Sobol; Y Nakamura; C Calmettes; J L Baulieu; J C Bigorgne; G Chabrier; J Couette; J L de Gennes; J Duprey
Journal:  Hum Genet       Date:  1989-11       Impact factor: 4.132

2.  Early diagnosis of multiple endocrine neoplasia type IIa.

Authors:  H P Neumann; O A Müller; B A Ponder; C G Mathew; H Telenius; W Schempp; C Schuemichen; N Freudenberg; P Schollmeyer
Journal:  Klin Wochenschr       Date:  1989-09-15

3.  Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.

Authors:  S Khosla; V M Patel; I D Hay; D J Schaid; C S Grant; J A van Heerden; S N Thibodeau
Journal:  J Clin Invest       Date:  1991-05       Impact factor: 14.808

4.  Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.

Authors:  S A Narod; M F Lavoué; K Morgan; C Calmettes; H Sobol; P J Goodfellow; G M Lenoir
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

5.  The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred.

Authors:  R M Landsvater; A G Rombouts; G J te Meerman; J M Schillhorn-van Veen; M J Berends; R A Geerdink; A Struyvenberg; C H Buys; C J Lips
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

6.  The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.

Authors:  N L Carson; J S Wu; C E Jackson; K K Kidd; N E Simpson
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

7.  The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.

Authors:  J S Wu; N L Carson; S Myers; A J Pakstis; J R Kidd; C M Castiglione; L Anderson; L S Hoyle; M Genel; M Verdy
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025
  7 in total

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