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Nature Genetics|February 19, 2003
Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemiaStephan M Tanner, Maria Aminoff, Fred A Wright, et al.
The Journal of Surgical Research|July 4, 2006
Differential gene expression in patients genetically predisposed to pancreatic cancerEmmanuel E Zervos, Stephan M Tanner, Dana A Osborne, et al.
Psychiatry Research|July 15, 2005
P50 inhibitory gating deficit is correlated with the negative symptomatology of schizophreniaSandrine Louchart-de la Chapelle, Daniel Levillain, Jean-François Ménard, et al.
The Journal of Clinical Endocrinology and Metabolism|June 21, 2013
In-depth characterization of the microRNA transcriptome in normal thyroid and papillary thyroid carcinomaMichal Swierniak, Anna Wojcicka, Malgorzata Czetwertynska, et al.
Cell|December 24, 1987
The sex-determining region of the human Y chromosome encodes a finger proteinD C Page, R Mosher, E M Simpson, et al.
Gene|September 5, 1998
Genomic structure of the human congenital chloride diarrhea (CLD) geneS Haila, P Höglund, S W Scherer, et al.
Human Molecular Genetics|July 1, 1993
Haplotype analysis to determine the position of a mutation among closely linked DNA markersM Ramsay, R Williamson, X Estivill, et al.
Scientific Reports|July 3, 2015
A germline mutation in SRRM2, a splicing factor gene, is implicated in papillary thyroid carcinoma predispositionJerneja Tomsic, Huiling He, Keiko Akagi, et al.
Thyroid : Official Journal of the American Thyroid Association|May 17, 2018
Identification of a Recurrent LMO7-BRAF Fusion in Papillary Thyroid CarcinomaHuiling He, Wei Li, Pearlly Yan, et al.
Genomics|May 1, 1990
Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologsD C Page, C M Disteche, E M Simpson, et al.
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