![Newborn screening / Cystic fibrosis / Prenatal diagnosis / Screening / Congenital adrenal hyperplasia due to 21-hydroxylase deficiency / Auditory neuropathy / Neonatology / Dried blood spot / Preterm birth / Health / Medicine / Pediatrics Newborn screening / Cystic fibrosis / Prenatal diagnosis / Screening / Congenital adrenal hyperplasia due to 21-hydroxylase deficiency / Auditory neuropathy / Neonatology / Dried blood spot / Preterm birth / Health / Medicine / Pediatrics](/pdf-icon.png)
| Document Date: 2012-07-24 10:12:47 Open Document File Size: 180,00 KBShare Result on Facebook
City Geneva / Shanghai / / Company Eaton / Norton / New York State Screening Laboratory / Duke Biochemical Genetics Laboratory / CVs / Carpenter / Sequenom / Genetic Disorders Group / Advanced Liquid Logic Inc. / / Continent America / Europe / / Country Germany / Switzerland / Netherlands / Malaysia / United States / Australia / United Kingdom / India / / Currency USD / / Event Diplomatic Relations / / Facility Children's Hospital of Fudan University / / IndustryTerm centers completed telephone surveys / clinical services / healthcare utilization / population-based carrier screening / imaging / recent search / carrier results / high throughput using common laboratory chemicals / software-assisted classification / extended cystic fibrosis carrier screening panel / prenatal carrier testing / web-survey / / MedicalCondition cystathionine beta synthase deficiency / atypical cystic fibrosis / congenital heart disease / congenital adrenal hyperplasia / Krabbe disease / only few diseases / urea cycle disorders / Cochrane Cystic Fibrosis / recurrent pancreatitis / nonclassical cystic fibrosis / rare inherited disorder / nasal polyps / _J_Cyst / congenital hearing loss / showed bilateral hearing loss / critical illness / extended cystic fibrosis / disorder / present severe diseases / sinusitis / otitis media / cystic fibrosis / metabolic disorders / MS / hearing loss / infections / classical cystic fibrosis / classic cystic fibrosis / Fabry disorders / hearing impairment / sepsis / haemoglobin disorders / Asthma / homocystinuria / hemoglobinopathies / premature birth / hemoglobinopathy screening / congenital heart defects / sickle cell diseases / severe combined immunodeficiency / disease / metabolic diseases / DOCK8 deficiency / malaria / chronic / carnitine uptake disorder / critical congenital heart defects / stroke / hormone deficiency / Allergy / mucopolysaccharidosis I / congenital sensorineural hearing loss / diseases / pathogenic cystic fibrosis / lysosomal storage diseases / Bilateral and unilateral sensorineural hearing loss / specific disease / sickle cell disease / SCID / respiratory insufficiency / inborn errors of metabolism / deficiency / genetic metabolic disorders / T cell lymphocytopenia / Meningitis / maple syrup urine disease / mild lung disease / disorders / glutaric aciduria type II / genetic disorders / / MedicalTreatment enzyme replacement therapies / counselling / antibiotic prophylaxis / enzyme replacement therapy / / Organization CF Foundation / CLIA Laboratory / Fudan University / American Academy / National Health Service / / Person Adamski / Lakshmi / Redman / / Position King / Major / genetic counselor / / Product DS / / ProvinceOrState Bali / Andhra Pradesh / Massachusetts / / SportsEvent nHL / / Technology Proteomics / tomography / transplantation / microfluidics / magnetic resonance imaging / genotype / /
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