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Genetic disorders
Results: 455

#	Item
201	Name of Study: Autism Spectrum Disorders Genetic Study Location: Vanderbilt University Medical Center, Nashville, TN Principal Investigator: Dr. Jonathan L. Haines Contact Information: Kelly A. Taylor, MS, CGC, Project M Add to Reading List Source URL: www.iancommunity.org Language: English - Date: 2009-03-26 16:29:46 Health Causes of autism Developmental disorder Seaver Autism Center Epidemiology of autism Autism Psychiatry Abnormal psychology
202	Public Comments to the Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:29 Rare diseases Medical genetics Epidemiology Newborn screening Inborn error of metabolism Screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Genetic counseling Guthrie test Medicine Health Pediatrics
203	Public Comment to the Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:17 Newborn screening Isovaleric acidemia Phenylketonuria Health Rare diseases Medicine
204	Advisory Committee on Heritable Disorders and Genetic Disease in Newborns and Children Subcommittee on Follow up and Treatment TM Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:28 Epidemiology Newborn screening Pediatrics Chronic Meditation Health Medicine Medical terms
205	Molecular Genetics Service Profile Achondrogenesis Type 1B (ACG1B) Introduction ◊ Add to Reading List Source URL: www.esdn.org Language: English - Date: 2009-03-19 12:03:51 Genetic testing Achondrogenesis Prenatal diagnosis DNA Prevention of Tay–Sachs disease Congenital disorders Medicine Health
206	Molecular Genetics Service Profile Spondyloepiphyseal dysplasia congenita (SEDC) Introduction ◊ ◊ Add to Reading List Source URL: www.esdn.org Language: English - Date: 2009-03-19 12:03:51 Congenital disorders Rare diseases Collagen disease Collagen type II alpha 1 Genes Spondyloepimetaphyseal dysplasia Spondyloepiphyseal dysplasia congenita Spondyloperipheral dysplasia Genetic testing Medicine Health Genetics
207	Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children Ronald Reagan Building and International Trade Center Washington, DC September 17-18, 2007 Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:16 Epidemiology Newborn screening Pediatrics
208	Newborn Screening Activities at the Centers for Disease Control and Prevention: An Update for the Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:39 Newborn screening Pediatrics Association of Public Health Laboratories Screening Health Medicine Epidemiology
209	Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children November 14, 2007 WEDNESDAY, NOVEMBER 14, 2007 2:00 P.M.—2:05 P.M. Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:12:52
210	The Etiology of ADHD: Behavioral and Molecular Genetic Approaches Erik Willcutt University of Colorado, Boulder Add to Reading List Source URL: psych.colorado.edu Language: English - Date: 2006-06-13 13:28:11 Childhood psychiatric disorders Health Attention Educational psychology Attention deficit hyperactivity disorder Dopamine transporter Methylphenidate Twin study Tourette syndrome Attention-deficit hyperactivity disorder Psychiatry Medicine

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