Literature DB >> 9630081

A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region.

A Mari1, F Amati, E Conti, M Bengala, G Novelli, B Dallapiccola.   

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Year:  1998        PMID： 9630081     DOI： 10.1111/j.1399-0004.1998.tb02683.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  2 in total

1.  Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.

Authors:  M Tassabehji; K Metcalfe; A Karmiloff-Smith; M J Carette; J Grant; N Dennis; W Reardon; M Splitt; A P Read; D Donnai
Journal:  Am J Hum Genet       Date:  1999-01       Impact factor: 11.025

2.  Simple, rapid and inexpensive quantitative fluorescent PCR method for detection of microdeletion and microduplication syndromes.

Authors:  Martin Stofanko; Higgor Gonçalves-Dornelas; Pricila Silva Cunha; Heloísa B Pena; Angela M Vianna-Morgante; Sérgio Danilo Junho Pena
Journal:  PLoS One       Date:  2013-04-19       Impact factor: 3.240
  2 in total

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