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A-Z Articles Index by First Author's Last Name

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Fackenthal JD et al. BRCA2 T2722R is a deleterious allele that causes exon skipping. Am J Hum Genet. 2002;71(3):625-31.

Fan et al. Survival motor neuron (SMN) protein: role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development. Hum Mol Genet 2002;11(14):1605-14.

Fan HC et al. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood. Proc Natl Acad Sci U S A. 2008 Oct 21;105(42):16266-71. Epub 2008 Oct 6.
Farasat S et al. Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA. 2009 Journal of Medical Genetics 46:103-111.

Feldkötter et al. Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy. Am J Hum Genet 2002;70:358-68.

Feng Y et al. Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis. Proc Natl Acad Sci U S A. 2006 Dec 26;103(52):19836-41. Epub 2006 Dec 15.
Foulquier F et al. Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.  Proc Natl Acad Sci U S A. 2006 Mar 7;103(10):3764-9
Frayling TM et al. A putative functional polymorphism in the IGF-I gene: association studies with type 2 diabetes, adult height, glucose tolerance, and fetal growth in U.K. populations. Diabetes. 2002 Jul;51(7):2313-6.
Freedman MS et al. Regulation of mammalian circadian behavior by non-rod, non-cone, ocular photoreceptors. Science. 1999; 284:502-4.
Frohling S et al. Identification of driver and passenger mutations of FLT3 by high-throughput DNA sequence analysis and functional assessment of candidate alleles. Cancer Cell. 2007 Dec;12(6): 501-513.
Frudakis T et al. Sequences associated with human iris pigmentation. Genetics. 2003 Dec;165(4):2071-83.