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Chest|February 15, 2001
Pulmonary dysfunction in adults with nephropathic cystinosisY Anikster, F Lacbawan, M Brantly, et al.American Journal of Medical Genetics|December 5, 2000
Clinical heterogeneity in mitochondrial DNA deletion disorders: a diagnostic challenge of Pearson syndromeF Lacbawan, C J Tifft, N L Luban, et al.Journal of Medical Genetics|January 24, 2007
Abnormal sterol metabolism in holoprosencephaly: studies in cultured lymphoblastsD Haas, J Morgenthaler, F Lacbawan, et al.Journal of Medical Genetics|October 4, 2005
Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotypeC Bendavid, B R Haddad, A Griffin, et al.The American Journal of Pathology|December 14, 1999
Familial encephalopathy with neuroserpin inclusion bodiesR L Davis, P D Holohan, A E Shrimpton, et al.Nature|October 12, 1999
Familial dementia caused by polymerization of mutant neuroserpinR L Davis, A E Shrimpton, P D Holohan, 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.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