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| Solomon BD, Bear KA, Wyllie A, et al. (2012) Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog. Journal of Medical Genetics. 49: 473-9 |
| Wannasilp N, Solomon BD, Warren-Mora N, et al. (2011) Holoprosencephaly in a family segregating novel variants in ZIC2 and GLI2. American Journal of Medical Genetics. Part A. 155: 860-4 |
| Keaton AA, Solomon BD, Kauvar EF, et al. (2010) TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype. Molecular Syndromology. 1: 211-222 |
| Solomon BD, Lacbawan F, Mercier S, et al. (2010) Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. Journal of Medical Genetics. 47: 513-24 |
| Lacbawan F, Solomon BD, Roessler E, et al. (2009) Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. Journal of Medical Genetics. 46: 389-98 |
| Findley SD, Tamanaha M, Clegg NJ, et al. (2003) Maelstrom, a Drosophila spindle-class gene, encodes a protein that colocalizes with Vasa and RDE1/AGO1 homolog, Aubergine, in nuage. Development (Cambridge, England). 130: 859-71 |
| Clegg NJ, Honda BM, Whitehead IP, et al. (1998) Suppressors of position-effect variegation in Drosophila melanogaster affect expression of the heterochromatic gene light in the absence of a chromosome rearrangement. Genome / National Research Council Canada = Gã©Nome / Conseil National De Recherches Canada. 41: 495-503 |
| Sinclair DA, Clegg NJ, Antonchuk J, et al. (1998) Enhancer of Polycomb is a suppressor of position-effect variegation in Drosophila melanogaster. Genetics. 148: 211-20 |
| Clegg NJ, Whitehead IP, Brock JK, et al. (1993) A cytogenetic analysis of chromosomal region 31 of Drosophila melanogaster. Genetics. 134: 221-30 |
| Clegg NJ, Whitehead IP, Williams JA, et al. (1993) A developmental and molecular analysis of Cdc2 mutations in Drosophila melanogaster. Genome / National Research Council Canada = GéNome / Conseil National De Recherches Canada. 36: 676-85 |