Literature DB >> 2864854

Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

P J Goodfellow, B N White, J J Holden, A M Duncan, E V Sears, H S Wang, L Berlin, K K Kidd, N E Simpson.   

Abstract

A DNA segment D20S5 isolated from a chromosome 19/20 flow-sorted library was shown to identify two restriction fragment length polymorphisms (RFLPs) with MspI and PvuII. The probe was localized by hybridization in situ to 20p12, the putative site of an interstitial deletion in some MEN 2A and 2B patients. Linkage of the D20S5 and MEN 2A loci was excluded at theta less than or equal to .13 using two large MEN 2A kindreds. These data suggest that the MEN 2A locus may not lie within 20p12 as previously suggested.

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Year:  1985        PMID： 2864854      PMCID： PMC1684696     

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


  28 in total

1.  Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.

Authors:  V M Riccardi; E Sujansky; A C Smith; U Francke
Journal:  Pediatrics       Date:  1978-04       Impact factor: 7.124

2.  Chromosomal deletion and retinoblastoma.

Authors:  A G Knudson; A T Meadows; W W Nichols; R Hill
Journal:  N Engl J Med       Date:  1976-11-11       Impact factor: 91.245

3.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

4.  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

5.  Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.

Authors:  J J Yunis; N K Ramsay
Journal:  J Pediatr       Date:  1980-06       Impact factor: 4.406

6.  Measurement of urinary epinephrine in screening for pheochromocytoma in multiple endocrine neoplasia type II.

Authors:  B P Hamilton; L Landsberg; R J Levine
Journal:  Am J Med       Date:  1978-12       Impact factor: 4.965

7.  Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Authors:  L M Mulligan; M A Phillips; C J Forster-Gibson; J Beckett; M W Partington; N E Simpson; J J Holden; B N White
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

8.  Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.

Authors:  U Francke; L B Holmes; L Atkins; V M Riccardi
Journal:  Cytogenet Cell Genet       Date:  1979

9.  Retinoblastoma and subband deletion of chromosome 13.

Authors:  J J Yunis; N Ramsay
Journal:  Am J Dis Child       Date:  1978-02

10.  Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatment.

Authors:  M W Partington; W R Ghent; E V Sears; N E Simpson
Journal:  Can Med Assoc J       Date:  1981-02-15       Impact factor: 8.262
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  8 in total

1.  Myotonic dystrophy and hyperparathyroidism: association with neurofibromatosis and multiple endocrine adenomatosis type 2A.

Authors:  N L Rosenberg; J H Diliberti; A M Andrews; N R Buist
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-12       Impact factor: 10.154

Review 2.  The map of chromosome 20.

Authors:  N E Simpson
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

3.  A DNA marker closely linked to the factor IX (haemophilia B) gene.

Authors:  L Mulligan; J J Holden; B N White
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

4.  Cytogenetic studies of individuals from four kindreds with multiple endocrine neoplasia type II syndrome.

Authors:  M G Butler; L J Rames; G M Joseph
Journal:  Cancer Genet Cytogenet       Date:  1987-10

5.  An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.

Authors:  L A Farrer; P J Goodfellow; C M Lamarche; I Franjkovic; S Myers; B N White; J J Holden; J R Kidd; N E Simpson; K K Kidd
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025

6.  High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndrome.

Authors:  M G Butler; D R Repaske; G M Joseph; J A Phillips
Journal:  Cancer Genet Cytogenet       Date:  1987-01

7.  Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome).

Authors:  S Schnittger; C Höfers; P Heidemann; F Beermann; I Hansmann
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

8.  The development of medullary carcinoma of the thyroid does not involve the loss of alleles on the short arm of chromosome 11.

Authors:  P M Broad; S Schifter; R K Craig
Journal:  Br J Cancer       Date:  1987-02       Impact factor: 7.640
  8 in total

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