Literature DB >> 9274580

Trinucleotide repeats not the only cause of anticipation.

F C Fraser1.   

Abstract

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Mesh：

Year:  1997        PMID： 9274580     DOI： 10.1016/S0140-6736(05)63077-2

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  13 in total

1.  Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.

Authors:  M C Lanasa; W A Hogge; C Kubik; J Blancato; E P Hoffman
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

Review 2.  A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome.

Authors:  Philip S Boonstra; Stephen B Gruber; Victoria M Raymond; Shu-Chen Huang; Susanne Timshel; Mef Nilbert; Bhramar Mukherjee
Journal:  Genet Epidemiol       Date:  2010-11       Impact factor: 2.135

3.  Elevated risk of chronic lymphocytic leukemia and other indolent non-Hodgkin's lymphomas among relatives of patients with chronic lymphocytic leukemia.

Authors:  Lynn R Goldin; Magnus Björkholm; Sigurdur Y Kristinsson; Ingemar Turesson; Ola Landgren
Journal:  Haematologica       Date:  2009-03-13       Impact factor: 9.941

4.  A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.

Authors:  M J Kovach; J P Lin; S Boyadjiev; K Campbell; L Mazzeo; K Herman; L A Rimer; W Frank; B Llewellyn; E W Jabs; D Gelber; V E Kimonis
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

5.  Clinical features of familial moyamoya disease.

Authors:  Rina Nanba; Satoshi Kuroda; Mitsuhiro Tada; Tatsuya Ishikawa; Kiyohiro Houkin; Yoshinobu Iwasaki
Journal:  Childs Nerv Syst       Date:  2005-09-30       Impact factor: 1.475

6.  Anticipation in familial pancreatic cancer.

Authors:  C D McFaul; W Greenhalf; J Earl; N Howes; J P Neoptolemos; R Kress; M Sina-Frey; H Rieder; S Hahn; D K Bartsch
Journal:  Gut       Date:  2005-06-21       Impact factor: 23.059

7.  Anticipation in familial Crohn's disease.

Authors:  B Grandbastien; M Peeters; D Franchimont; C Gower-Rousseau; D Speckel; P Rutgeerts; J Belaïche; A Cortot; R Vlietinck; J F Colombel
Journal:  Gut       Date:  1998-02       Impact factor: 23.059

8.  [Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families].

Authors:  A M Siegel; H Bertalanffy; J J Dichgans; C E Elger; H Hopf; N Hopf; M Keidel; A Kleider; G Nowak; R A Pfeiffer; J Schramm; S Spuck; H Stefan; U Sure; C R Baumann; G A Rouleau; D J Verlaan; E Andermann; F Andermann
Journal:  Nervenarzt       Date:  2005-02       Impact factor: 1.214

9.  Epilepsy in families: Age at onset is a familial trait, independent of syndrome.

Authors:  Colin A Ellis; Leonid Churilov; Michael P Epstein; Sharon X Xie; Susannah T Bellows; Ruth Ottman; Samuel F Berkovic
Journal:  Ann Neurol       Date:  2019-05-20       Impact factor: 10.422

10.  The International Testicular Cancer Linkage Consortium: a clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred.

Authors:  Phuong L Mai; Michael Friedlander; Kathy Tucker; Kelly-Anne Phillips; David Hogg; Michael A S Jewett; Radka Lohynska; Gedske Daugaard; Stéphane Richard; Catherine Bonaïti-Pellié; Axel Heidenreich; Peter Albers; Istvan Bodrogi; Lajos Geczi; Edith Olah; Peter A Daly; Parry Guilford; Sophie D Fosså; Ketil Heimdal; Ludmila Liubchenko; Sergei A Tjulandin; Hans Stoll; Walter Weber; Douglas F Easton; Darshna Dudakia; Robert Huddart; Michael R Stratton; Lawrence Einhorn; Larissa Korde; Katherine L Nathanson; D Timothy Bishop; Elizabeth A Rapley; Mark H Greene
Journal:  Urol Oncol       Date:  2009-01-22       Impact factor: 3.498
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