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American Journal of Medical Genetics|December 5, 2000
Phenotypic features in a boy with monosomy 18 mosaicismK E Jackson, F Tsien, M MarbleGenetic Counseling (Geneva, Switzerland)|January 22, 2005
Trisomy 1q43 syndrome: a consistent phenotype with macrocephaly, characteristic face, developmental delay and cardiac anomaliesE Morava, K E Jackson, F Tsien, et al.Cancer Genetics and Cytogenetics|April 1, 1997
der(1)t(1;19)(p12;p11): a new nonrandom chromosomal abnormality in myelodysplastic syndromeJ I Gill, M Varela, F Tsien, et al.Molecular Genetics and Metabolism|November 16, 2001
Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissuesF Tsien, B Sun, N E Hopkins, et al.Cytogenetic and Genome Research|February 14, 2003
Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangementsF Tsien, E S Fiala, B Youn, et al.Cytogenetics and Cell Genetics|July 15, 2000
DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patientsC M Tuck-Muller, A Narayan, F Tsien, et al.American Journal of Human Genetics|May 1, 1994
Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implicationsJ Leana-Cox, L Jenkins, C G Palmer, et al.Human Reproduction (Oxford, England)|February 1, 1994
The relationship of initial embryo crown--rump length to pregnancy outcome and abortus karyotype based on new growth curves for the 2-31 mm embryoR P Dickey, R F Gasser, T T Olar, et al.Cell Death and Differentiation|January 28, 2012
IL-7Rα deficiency in p53null mice exacerbates thymocyte telomere erosion and lymphomagenesisR Kibe, S Zhang, D Guo, et al.Human Molecular Genetics|December 14, 2001
DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genesM Ehrlich, K L Buchanan, F Tsien, et al.Pageof 1