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X chromosome
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#	Item
31	PDF Document Add to Reading List Source URL: www.esp.org Language: English - Date: 2010-05-11 22:25:57 Chromosomes Molecular genetics Cell biology Chromatin Chromomere Homologous chromosome Prophase X chromosome Synapsis Biology Genetics Cytogenetics
32	Autism research news and opinion 23 September 2014 – 30 September 2014 For the latest news, visit SFARI.org on the Web Rousing silenced X chromosome may treat Rett syndrome Jessica Wright Add to Reading List Source URL: simonsfoundation.s3.amazonaws.com Language: English - Date: 2014-09-30 09:44:30 Abnormal psychology Neurological disorders Pervasive developmental disorders Communication disorders Syndromes Rett syndrome MECP2 Angelman syndrome Heritability of autism Health Autism Psychiatry
33	Company noCharity noRare Chromosome Disorder Support Group Report and Financial Statements Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2010-10-28 06:44:13 Chromosome Social networking service Aware Karyotype Genetic testing X chromosome Genetics Biology Cytogenetics
34	Company noCharity noRare Chromosome Disorder Support Group Report and Audited Financial Statements Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2011-11-15 10:32:39 Chromosome X chromosome Genetic disorder Karyotype Isodicentric 15 The Focus Foundation Genetics Biology Cytogenetics
35	Archer H, Evans J, Leonard H, Colvin L, Ravine D, Christodoulou J, Williamson S, Charman T, Bailey ME, Sampson J, de Klerk N, Clarke A. Correlation between clinical severity in patients with Rett syndrome with a p.R168X Add to Reading List Source URL: www.aussierett.org.au Language: English - Date: 2011-09-30 03:33:06 Cytogenetics Syndromes Neurological disorders Epigenetics Rett syndrome MECP2 X-inactivation X chromosome Mutation Biology Genetics Philosophy of biology
36	Archer H, Evans J, Leonard H, Colvin L, Ravine D, Christodoulou J, Williamson S, Charman T, Bailey ME, Sampson J, de Klerk N, Clarke A. Correlation between clinical severity in patients with Rett syndrome with a p.R168X Add to Reading List Source URL: www.interrett.org.au Language: English - Date: 2011-09-30 03:33:06 Cytogenetics Syndromes Neurological disorders Epigenetics Rett syndrome MECP2 X-inactivation X chromosome Mutation Biology Genetics Philosophy of biology
37	THE FRAGILE X SOCIETY FRAGILE X SYNDROME: MALE CARRIERS OF FRAGILE X INTRODUCTION Add to Reading List Source URL: fragilex.org.au Language: English - Date: 2013-04-03 19:37:41 Biology Neurological disorders Syndromes Fragile X syndrome Mental retardation Pediatrics FMR1 X chromosome Sherman paradox Genetics Health Autism
38	PDF Document Add to Reading List Source URL: www.qcidd.com.au Language: English - Date: 2013-07-26 01:29:43 Neurological disorders Autism Fragile X syndrome Mental retardation Pediatrics FMR1 Down syndrome X chromosome Turner syndrome Health Syndromes Genetics
39	You are not alone Fragile X Syndrome is the most common inherited cause of intellectual disability and cognitive impairment worldwide. Add to Reading List Source URL: fragilex.org.au Language: English - Date: 2013-03-05 21:38:48 Syndromes Neurological disorders Abnormal psychology Pediatrics Fragile X syndrome Mental retardation Sex linkage Turner syndrome X chromosome Health Autism Medicine
40	Microsoft Word - FB_Book_CCasal_Genetics_RP14072010_JG.doc Add to Reading List Source URL: fishbase.mnhn.fr Language: English - Date: 2012-03-20 20:11:23 Centromere Chromosome Karyotype Polyploid Fluorescence in situ hybridization X chromosome Acentric fragment Ploidy DNA Genetics Biology Cytogenetics