Applying Genomic Analysis to Newborn Screening

per Solomon, B.D., Pineda-Alvarez, D.E., Bear, K.A., Mullikin, J.C., Evans, J.P.
Publicat 2012

High Intellectual Function in Individuals with Mutation-Positive Microform Holoprosencephaly

per Solomon, B.D., Pineda-Alvarez, D.E., Gropman, A.L., Willis, M.J., Hadley, D.W., Muenke, M.
Publicat 2012

A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in Humans

per Arauz, R.F., Solomon, B.D., Pineda-Alvarez, D.E., Gropman, A.L., Parsons, J.A., Roessler, E., Muenke, M.
Publicat 2010

Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL Association

per Solomon, B.D., Pineda-Alvarez, D.E., Hadley, D.W., Hansen, N.F., Kamat, A., Donovan, F.X., Chandrasekharappa, S.C., Hong, S.-K., Roessler, E., Mullikin, J.C.
Publicat 2013

TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype

per Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R., Gowans, G.C., Clegg, N.J, Delgado, M.R., Hahn, J.S., Pineda-Alvarez, D.E., Lacbawan, F., Vélez, J.I., Roessler, E., Muenke, M.
Publicat 2011