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Molecular Syndromology|May 9, 2013
Mitochondrial Factors and VACTERL Association-Related Congenital MalformationsS Siebel, B D SolomonMolecular Syndromology|November 1, 2012
Applying Genomic Analysis to Newborn ScreeningB D Solomon, D E Pineda-Alvarez, K A Bear, et al.Molecular Syndromology|November 1, 2012
High Intellectual Function in Individuals with Mutation-Positive Microform HoloprosencephalyB D Solomon, D E Pineda-Alvarez, A L Gropman, et al.Molecular Syndromology|November 4, 2010
A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in HumansR F Arauz, B D Solomon, D E Pineda-Alvarez, et al.Molecular Syndromology|May 9, 2013
Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL AssociationB D Solomon, D E Pineda-Alvarez, D W Hadley, et al.Molecular Syndromology|November 30, 2011
TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and PhenotypeA A Keaton, B D Solomon, E F Kauvar, et al.Molecular Psychiatry|June 20, 2012
Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's diseaseJ I Vélez, S C Chandrasekharappa, E Henao, et al.Journal of Medical Genetics|April 7, 2009
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and functionF Lacbawan, B D Solomon, E Roessler, et al.Pageof 1