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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 1, 1991
Flow cytometric analysis of DNA ploidy and S-phase fraction in breast cancer using cells obtained by ex vivo fine-needle aspiration: an optimal method for sample collectionC A Eliasen, L M Opitz, E C Vamvakas, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndromeMarcella Zollino, Rosetta Lecce, Angelo Selicorni, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2011
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndromeSarah B Pierce, Karen M Chisholm, Eric D Lynch, et al.
Human Genetics|January 1, 1981
The "cat eye syndrome": dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical pictureA Schinzel, W Schmid, M Fraccaro, et al.
American Journal of Human Genetics|August 27, 1998
Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domainK Gaudenz, E Roessler, N Quaderi, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndromeFernanda Sarquis Jehee, Carla Rosenberg, Ana Cristina Krepischi-Santos, et al.
Gynecologic Oncology|December 14, 2012
A novel curcumin-based vaginal cream Vacurin selectively eliminates apposed human cervical cancer cellsPriya Ranjan Debata, Mario R Castellanos, Jimmie E Fata, et al.
Scientific Reports|January 14, 2018
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C SyndromeRoser Urreizti, Sarah Damanti, Carla Esteve, et al.
Molecular Systems Biology|June 6, 2020
High-throughput, microscope-based sorting to dissect cellular heterogeneityNicholas Hasle, Anthony Cooke, Sanjay Srivatsan, et al.
American Journal of Medical Genetics|January 1, 1981
Further delineation of the C (trigonocephaly) syndromeR M Antley, D S Hwang, W Theopold, et al.
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