The Raymond C. Philips Research and Education Unit (RCPU) was established in 1978, as outlined in section 393.20 of the Florida Statutes (now F.S. 393.064) of what is entitled the “prevention” legislation. The Unit is named for Mr. Philips, who was a well-known administrator and superintendent of Gainesville’s Tacachale (previously called Sunland Training Center) for thirty-eight years.
Goals of the RCPU
The RCPU was established for the purpose of the prevention, treatment and amelioration of developmental disabilities. The unit provides service, education and prevention efforts through the following methods:
- Research into the etiology of developmental disabilities;
- Diagnosis of unusual conditions and syndromes associated with a developmental disability in persons identified through the Department of Children and Families and the Department of Health. The Unit conducts genetic evaluations in the outpatient clinic at Tacachale and at other locations in the state;
- Evaluation of families affected with a developmental disability of genetic origin in order to provide them with genetic counseling aimed at prevention of the recurrence of the disorder in other family members;
- Training for professionals throughout the state in the areas of genetics and developmental disabilities. The RCPU provides educational seminars, conferences, and lectures on developmental disabilities throughout the state. To arrange for a session to be held in your area, contact the Division of Genetics at (352) 294-5050.
- Dissemination of new knowledge throughout the Department of Health, especially those offices in the Department of Children and Families:
R.C. Philips Newsletter Archive
- Propionic Acidemia
Vol. XXXV No. 2; June 2024 - Dravet Syndrome
Vol. XXXVI No. 1; June 2024 - An Overview of Coffin Siris Syndrome and ARID1B-Related Disorders
Vol. XXXV No. 1; December 2023 - EFTUD2-related Mandibulofacial Dysostosis with Microcephaly
Vol. XXXIV No. 2; June 2023 - Duchenne Muscular Dystrophy
Vol. XXXIV No.1; December 2022 - Advancements in Genetic Testing
Vol. XXXIII No. 2; June 2022 - Kabuki Syndrome
Vol. XXXIII No. 1; December 2021 - KAT6A-Related Disorder
Vol. XXXII, No. 2; June 2021 - Russell Silver syndrome
Vol. XXXII, No. 1; December 2020 - Sex Chromosome Abnormalities
Vol. XXXI, No. 2; June 2020 - Trisomy 13 and Trisomy 18
Vol. XXXI, No.1; December 2019 - Newborn Screening Update
Vol. XXX No.2; June 2019 - Down Syndrome Updates
Vol. XXX No.1; December 2018 - Metabolism Clinic Updates
Vol. XXIX No.2; June 2018 - Coping with a new diagnosis
Vol. XXIX No.1; December 2017 - Phenylalanine Hydroxylase (PAH) Deficiency
Vol. XXVIII No.2; June 2017 - Cornelia de Lange Syndrome
Vol. XXVIII No.1; December 2016 - A Phenotypic Review of Connective Tissue and Related Disorders
Vol. XXVII No. 2; June, 2016 - Smith Lemli Opitz Syndrome
Vol. XXVII No. 1; December, 2015 - Genetic hearing loss in the pediatric setting: Common genetic etiologies, testing, and counseling implications
Vol. XXVI No. 2; June, 2015 - Reproductive counseling in the modern era: The expanding role of cell free DNA (cfDNA) and non-invasive prenatal screening (NIPS)
Vol. XXVI No. 1; December, 2014 - Chromosome Microdeletions and Microduplications – New Syndromes Identified by New Technologies
Vol. XXV No. 2; June, 2014
- Family Medical History: Why it Matters
Vol. XXV No. 1; May, 2014 - Cognitive, Behavioural, and Psychiatric Manifestations of 22q11.2 Deletion Syndrome
Vol. XXIV No. 2; June, 2013 - Next Generation Sequencing-Broadening the Horizon For Genetic Testing
Vol. XXIV No. 1; May, 2013 - Fragile X and Linkage to Autism
Vol. XXIII No. 2; June, 2012 - Molecular Biology of Epilepsy Genes
Vol. XXIII No. 1; January, 2012 - Coping with the Genetic Diagnosis
Vol. XXII No. 2; June, 2011 - Looks like Angelman syndrome but isn’t – What is in the differential?
Vol. XXII No. 1; January, 2011 - Chromosomes and Beyond…new Technologies for Genetic Testing
Vol. XXI No. 2; July 2010 - Genetics of Autism
Vol. XXI No. 1; July 2009 - Noonan Syndrome
Vol. XX No. 2; Jan 2009 - Macrocephaly Disorders
Vol. XX No. 1; Aug 2008 - Hearing loss
Vol. XIX No. 2; Jan 2008 - Beckwith Wiedemann Syndrome
Vol. XIX No. 1; July 2007 - Expanded Newborn Screening in Florida
Vol. XVIII No. 2; January 2007 - Review of Genetic Testing Techniques
Vol. XVII No. 2; January 2006 - Tuberous Sclerosis
Vol. XVII No. 1; July 2005 - DiGeorge Syndrome/Velo-Cardio-Facial Syndrome
Vol. XVI No. 2; Jan 2005 - Williams Syndrome
Vol. XVI No. 1; Jul 2004 - Neural Tube Defects
Vol. XIII No. 2; Dec 2000 - Hunting for Genes
Vol. XIII No. 1; Jun 2000