Literature DB >> 11836368

Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation in two sisters: a new autosomal recessive MCA/MR syndrome?

J Siegel-Bartlet, A Levin, A S Teebi, S J Kennedy.   

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Year:  2002        PMID： 11836368      PMCID： PMC1735031          DOI： 10.1136/jmg.39.2.145

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  1 in total

1.  The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.

Authors:  Paul G Matteson; Jigar Desai; Ron Korstanje; Gloria Lazar; Tanya E Borsuk; Jarod Rollins; Sindhuja Kadambi; Jamie Joseph; Taslima Rahman; Jason Wink; Rym Benayed; Beverly Paigen; James H Millonig
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-04       Impact factor: 11.205
  1 in total

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