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Genetic disorders
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#	Item
71	Current Status of Genetic Studies of Exocrine Pancreatic Insufficiency in Dogs Add to Reading List Source URL: www.2ndchance.info Language: English - Date: 2014-02-04 19:23:38 Genetic epidemiology Genome-wide association study Dog leukocyte antigen Genetic disorder German Shepherd Dog Doberman Pinscher Genetic linkage Exocrine pancreatic insufficiency Biology Genetics Pancreas disorders
72	Tay-Sachs Disease and other conditions more common in the Ashkenazi Jewish community Fact Sheet 35 Important points   Add to Reading List Source URL: www.genetics.edu.au Language: English - Date: 2015-03-29 18:44:37 Rare diseases Medical genetics Lipid storage disorders Tay–Sachs disease Genetic disorder Familial dysautonomia Recessive Cystic fibrosis Genetic testing Health Medicine Genetics
73	The Cardiac Society of Australia and New Zealand Guidelines for Genetic Testing of Inherited Cardiac Disorders Development of this guideline by Ms Poonam Zodgekar, Ms Jodie Ingles, Ms Laura Yeates, Mr Ivan Macciocca, A/ Add to Reading List Source URL: www.csanz.edu.au Language: English - Date: 2015-01-26 21:57:44 Medical genetics Syndromes Cardiomyopathy Channelopathy Hypertrophic cardiomyopathy Genetic testing Arrhythmogenic right ventricular dysplasia Predictive testing Genetic counseling Medicine Health Cardiac dysrhythmia
74	WORLD ARABIAN HORSE ORGANIZATION GENETIC DISORDERS IN ARABIAN HORSES: CURRENT RESEARCH PROJECTS . GENERAL INTRODUCTION: Researchers have already identified over 13,000 genetically inherited traits in humans, more than 5, Add to Reading List Source URL: ahsa.asn.au Language: English - Date: 2014-03-05 01:59:45 American Quarter Horses Rare diseases Horse coat colors Lavender Foal Syndrome Arabian horse Severe combined immunodeficiency Cerebellar abiotrophy Hyperkalemic periodic paralysis Gray Health Equidae Biology
75	Dragica Radojković, PhD Dragica Radojković, PhD is a molecular biologist with the expertise in human molecular genetics. She is in charge of genetic testing for cystic fibrosis, CFTR related disorders, thrombophilia a Add to Reading List Source URL: epmanet.eu Language: English - Date: 2012-12-17 17:42:48 Pediatrics Genetics Biology Polymorphism Health Channelopathy Cystic fibrosis
76	Australian Paediatric Surveillance Unit Add to Reading List Source URL: www.apsu.org.au Language: English - Date: 2012-12-19 00:55:11 Pervasive developmental disorders Communication disorders Neurological disorders Syndromes Autism Rett syndrome MECP2 Genetic disorder Medical genetics Medicine Health Biology
77	Tracing Genetic Traits in Your Family While I wish we could trace genetically determined behavioral traits in your family, much less is known about the genetics of behavior, with the exception of genetic disorders that h Add to Reading List Source URL: www.uni.edu Language: English - Date: 2011-01-26 10:56:42 Dominance Mendelian inheritance Phenotype Phenotypic trait Genotype Introduction to genetics Human genetics Monohybrid cross Classical genetics Genetics Recessive
78	doi:[removed]scan/nsq059 SCAN[removed], 203^211 Is there a genetic contribution to cultural differences? Collectivism, individualism and Add to Reading List Source URL: www.scn.ucla.edu Language: English - Date: 2014-08-20 17:18:23 Genetic genealogy Abnormal psychology Mood disorders 5-HTTLPR Serotonin transporter Human genetic variation Major depressive disorder Allele frequency Genetic drift Biology Population genetics Genetics
79	World Rare Disease Day 28 February 2011 World Rare Disease Day is a global event held annually on the last day of February. Its main objective is to raise awareness of rare diseases and their impact on not only the kids Add to Reading List Source URL: www.awch.org.au Language: English - Date: 2014-01-18 05:49:10 Medicine Lipid storage disorders Rare Disease Day European Organization for Rare Diseases Fabry disease Orphan drug Disease Genetic Alliance UK Health Epidemiology Rare diseases
80	Novel techniques for the prevention of mitochondrial DNA disorders: an ethical review Inherited genetic disorders caused by mutations in mitochondrial DNA can cause a wide range of severely debilitating and disabling hea Add to Reading List Source URL: nuffieldbioethics.org Language: English - Date: 2015-02-02 05:54:06 Mitochondrial disease DNA Cryobiology Medical genetics Mitochondrion Human Fertilisation and Embryology Authority Spindle transfer Mitochondrial DNA In vitro fertilisation Biology Genetics Fertility medicine

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