essentialmedgen.com
essentialmedgen
http://www.essentialmedgen.com/Patient-support-directories.php
Links to databases and analysis tools. Directories of gene testing labs. Genome browsers and scientific information re genes and proteins. Tools for DNA and protein sequence analysis. Websites useful when designing primers. Analysis of functional signficance of missense mutations. Human Genome Project: ethics and education. Updates and additional information. How "silent" mutations may not be silent. Fragile X premutations: pathogenic mechanism. Nov 2012: 1000 Genomes Project. Q009 Tumour suppressor genes.
essentialmedgen.com
essentialmedgen
http://www.essentialmedgen.com/Computer-aided-syndrome-diagnosis.php
Links to databases and analysis tools. Directories of gene testing labs. Genome browsers and scientific information re genes and proteins. Tools for DNA and protein sequence analysis. Websites useful when designing primers. Analysis of functional signficance of missense mutations. Human Genome Project: ethics and education. Updates and additional information. How "silent" mutations may not be silent. Fragile X premutations: pathogenic mechanism. Nov 2012: 1000 Genomes Project. Q009 Tumour suppressor genes.
ophthalmreviews.com
FACE2 GENE – НОВА ВЪЗМОЖНОСТ ЗА РАННА И СВОЕВРЕМЕННА ДИАГНОЗА ...
https://ophthalmreviews.com/p/face2-gene-нова-възможност-за-ранна-и-своевременна-диагноза-на-дисморфични-очни-синдроми-а-поповаp
FACE2 GENE НОВА ВЪЗМОЖНОСТ ЗА РАННА И СВОЕВРЕМЕННА ДИАГНОЗА НА ДИСМОРФИЧНИ ОЧНИ СИНДРОМИ - А. Попова. Детски очен кабинет, УМБАЛ Александровска , МУ София. Ранната и своевременна диагностика на дисморфичните синдроми продължава да е истинско изпитание и предизвикателство за педиатри, офталмолози, клинични генетици, дисморфолози. Над 80 % от дисморфичните синдроми имат различни очни прояви. Провежда се литературна справка за. FACE2 GENE и се споделя личен опит. FACE2 GENE, чрез. Генетици от целия свят.
ophthalmreviews.com
ОФТАЛМ РЕВЮ >>>>
https://ophthalmreviews.com/статии/офталм-ревю
ТРАНСПЛАНТАЦИЯ НА АМНИОТИЧНА МЕМБРАНА ЛОГИСТИКА, ХИРУРГИЧЕСКИ ХАРАКТЕРИСТИКИ, ТЕХНИКИ И И МИКРОСТРУКТУРЕН АНАЛИЗ НА РЕЗУЛТАТИТЕ - д-р Яна Манолова Манолова, проф. д-р. Христина Николова Групчева, д.м.н. Трансплантация на амниотична мембрана - логистика, хирургически техники и микроструктурен анализ на резултатите. A пия към МУ-Варна. В зависимост от тежестта на обективната симптоматика и вида на заболяването е извършена трансплантация тип покритие и/или пълнител в един, два или повече слоя. Напра...OCT е...
drsref.com.au
Medical Software DrsRef
http://www.drsref.com.au/medsoftware.html
Medical Software and eHealth. ADHA Australian Digital Health Agency. Pictures Of Standard Syndromes and Undiagnosed Malformations. [Victorian Clinical Genetics Service (VCGS) and the Murdoch Childrens Research Institute (MCRI) ]. PRM's - Patient Reported Measures. Agency for Clinical Innovation [NSW Govt]. Integrates with Best Practice, Pracsoft, ZedMed and Genie. Integrates with practice software. 7 Myths of Online Appts. Links GPs with Specialists via video. IoSafe Data Recovery Service. Go To My PC.
geneticandrarediseasenetwork.org.au
Health Professionals - Genetic and Rare Disease Network - Helping genetic & rare disease support groups deliver quality support and services to individuals and families affected by genetic and rare conditions
http://www.geneticandrarediseasenetwork.org.au/health-professionals
Genetic and Rare Disease Network Logo. Formerly the Genetic Support Council of WA. Skip to Page Content. What is a genetic condition? What is a rare disease? Resources for Parents and Families. Red Flags for Genetic and Rare Disease. Genetic and Rare Disease Health Professional Register. Dr Mark Thomas - Nephrologist. Professor Stephan Schug - Anaesthesiology and Pain Medicine. Dr Merrilee Needham - Consultant Neurologist. Dr Melanie Wong - Paediatric Allergist and Immunologist. Dr Amali Mallawaarachchi ...
segcd.org
SEGCD - Sociedad Española de Genética Clínica y Dismorfología :: Enlaces
http://www.segcd.org/enlaces
C/ Universidad, 4. SECRETARÍA TÉCNICA. GRUPO GEYSECO, S.L. Sociedades de Genética de interés:. Asociación Española de Genética Humana:. European Society of Human Genetics:. The Clinical Genetics Society (CGS):. American College of Medical Genetics:. Página de Genética de la Universidad de Kansas. Recursos de apoyo al diagnóstico de interés:. McKusick s Mendelian Inheritance in Man:. Wwwncbi.nlm.nih.gov/omim/. Http:/ www.ncbi.nlm.nih.gov/sites/GeneTests/? Asociación Española de Pediatría:.
