| Neri G, Opitz JM
Down syndrome: Comments and reflections on the 50th anniversary of Lejeune's discovery. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 17.
Abstract | Full Citation | Find Related Articles | | Lehman VT, Patterson MC, Babovic-Vuksanovic D, et al.
Cerebral and cerebellar white matter abnormalities with magnetic resonance imaging in a child with Feingold syndrome. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation | Find Related Articles | | Wada Y, Nishimura G, Nagai T, et al.
Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia and acampomelic campomelic dysplasia. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Full Citation | Find Related Articles | | Mademont-Soler I, Morales C, Madrigal I, et al.
Prenatal diagnosis of two different unbalanced forms of an inherited (Y;12) translocation. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation | | Gaston-Massuet C, Kelberman D, Dattani M, et al.
Absence of SIX3 mutations in patients with congenital hypopituitarism. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Full Citation | Find Related Articles | | De Souza E, Halliday J, Chan A, et al.
Recurrence risks for trisomies 13, 18, and 21. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation | Find Related Articles | | Schneider A, Bardakjian T, Reis LM, et al.
Novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation | Find Related Articles | | Andrieux J, Dubourg C, Rio M, et al.
Genotype-phenotype correlation in four 15q24 deleted patients identified by array-CGH. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation | Find Related Articles | | Shkalim V, Baris HN, Gal G, et al.
Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach-Rott syndrome. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation | Find Related Articles | | Chen W, Kim MS, Shanbhag S, et al.
The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: Quadricuspid aortic valve and other midline defects. [JOURNAL ARTICLE]
Am J Med Genet A 2009 Nov 16.
Abstract | Full Citation |   |
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