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Ang GS, Simpson SA, Reddy AR 
Mycophenolate mofetil embryopathy may be dose and timing dependent. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 20.
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Bailey DB, Raspa M, Olmsted M, et al. 
Co-occurring conditions associated with FMR1 gene variations: Findings from a national parent survey. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 20.
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Fraser FC 
Of mice and children: Reminiscences of a teratogeneticist. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 19.
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Brunetti-Pierri N, Sahoo T, Frioux S, et al. 
15q13q14 deletions: Phenotypic characterization and molecular delineation by comparative genomic hybridization. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 17.
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Izumi K, Yamashita Y, Aramaki M, et al. 
Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 17.
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Adegbite NS, Xu M, Kaplan FS, et al. 
Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS-based heterotopic ossification. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 13.
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Bianca S, Boemi G, Barrano B, et al. 
Mosaic trisomy 20: Considerations for genetic counseling. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 13.
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Kamoun-Goldrat A, Martinovic J, Saada J, et al. 
Prenatal cortical hyperostosis with COL1A1 gene mutation. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 13.
Abstract | Full Citation
Martínez-Frías ML 
The balance of nature: Reflections on the physics and mathematics structure of the living world and the human genome. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 13.
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Digilio MC, Calzolari F, Capolino R, et al. 
Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome). [JOURNAL ARTICLE]
Am J Med Genet A 2008 Jun 13.
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