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Noonan syndrome
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21	What is 22q11.2 Deletion Syndrome? 22q11.2 deletion syndrome is a genetic condition that affects learning, health, and physical traits. It occurs in males and females of all racial and ethnic backgrounds. 22q11.2 deletio Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:49:08 Marfan syndrome DiGeorge syndrome Angelman syndrome Down syndrome Genetic disorder Turner syndrome Noonan syndrome Genetic counseling Developmental disorder Health Syndromes Beckwith–Wiedemann syndrome
22	Microsoft Word - CCHD Provider info for the Website[removed]docx Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2012-10-01 08:28:56 Circulatory system Congenital heart defect Cardiology Noonan syndrome Ventricular septal defect Fetal echocardiography Congenital heart disease Health Medicine
23	A single red heart with reflection. Add to Reading List Source URL: www.agrenska.se Language: English - Date: 2013-09-19 05:36:44 Genetic genealogy Medical genetics Noonan syndrome Unity Congenital heart defect Costello syndrome Health Syndromes Genodermatoses
24	Rare Disorders of the MAPK pathway; Current status/ future directions Add to Reading List Source URL: www.eshg.org Language: English - Date: 2012-05-11 05:09:17 Genodermatoses Syndromes Noonan syndrome Medical genetics LEOPARD syndrome Virtual Global University Hypertrophic cardiomyopathy Medicine Health Genetic genealogy
25	Noonan Syndrome Genetic Testing Interpretation Order Form Add to Reading List Source URL: www.asperbio.com Language: English - Date: 2013-08-28 08:19:51 Medical genetics Genodermatoses Body shape Noonan syndrome Dysmorphic feature Health Syndromes Genetic genealogy
26	3rd InternaHonal MeeHng on GeneHc Syndromes of the Ras/MAPK Pathway: Towards a TherapeuHc Approach Poster Abstracts Add to Reading List Source URL: www.cfcsyndrome.org Language: English - Date: 2013-08-11 16:01:59 Genodermatoses Neuro-cardio-facial-cutaneous syndromes Syndromes Neurological disorders Noonan syndrome LEOPARD syndrome Developmental neuroscience PTPN11 Costello syndrome Health Medicine Genetic genealogy
27	Third International Meeting on Genetic Syndromes of the Ras/MAPK Pathway: Towards a Therapeutic Approach Renaissance Orlando at SeaWorld Add to Reading List Source URL: www.cfcsyndrome.org Language: English - Date: 2013-08-11 16:01:54 Genetic genealogy Neuro-cardio-facial-cutaneous syndromes Syndromes Neurological disorders Developmental neuroscience Costello syndrome Neurofibromatosis Noonan syndrome Cardiofaciocutaneous syndrome Health Medicine Genodermatoses
28	Product catalogue[removed]Days from Sample to Statement Add to Reading List Source URL: blueprintgenetics.com Language: English - Date: 2014-05-07 06:36:57 Medical genetics Syndromes Neuro-cardio-facial-cutaneous syndromes Cardiomyopathy Cardiovascular disease Noonan syndrome Arrhythmogenic right ventricular dysplasia Desmoplakin Costello syndrome Genodermatoses Health Genetic genealogy
29	The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genetic genealogy Neuro-cardio-facial-cutaneous syndromes Syndromes Neurological disorders Developmental neuroscience LEOPARD syndrome Neurofibromatosis type I Noonan syndrome Neurofibroma Medicine Health Genodermatoses
30	Crystal structures from the Plasmodium peroxiredoxins: new insights into oligomerization and product binding Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genetics Biochemistry Genes PTPN11 SH2 domain Protein tyrosine phosphatase Mitogen-activated protein kinase Noonan syndrome Phosphoinositide 3-kinase Biology Protein domains Signal transduction

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