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Biotinidase
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51	National Newbor n Screening 2006 Incidence Repor t Tabulated incidence data for Newborn Screening Disorders organized by State and Genetics and Newborn Screening Regional Collaborative Groups National Newborn Screening Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-02-23 16:20:53 Mental retardation Epidemiology Newborn screening Medical specialties Biotinidase deficiency Medical genetics Galactosemia Association of Public Health Laboratories Phenylketonuria Medicine Health Pediatrics
52	National Newbor n Screening 2002 Incidence Repor t Tabulated incidence data for Newborn Screening Disorders organized by State and Genetics and Newborn Screening Regional Collaborative Groups National Newborn Screening Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-02-23 16:22:56 Mental retardation Epidemiology Newborn screening Medical specialties Biotinidase deficiency Medical genetics Galactosemia Phenylketonuria Association of Public Health Laboratories Medicine Health Pediatrics
53	NATIONAL NEWBORN SCREENING REPORT[removed]Final Report: July, 2002 National Newborn Screening Report[removed] Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2002-08-01 08:21:14 Rare diseases Epidemiology Newborn screening Adrenal gland disorders Intersexuality Galactosemia Congenital adrenal hyperplasia Biotinidase deficiency Cystic fibrosis Health Medicine Pediatrics
54	Biotinidase Deficiency Biotinidase deficiency is an autosomal recessive inherited disorder that results in the inability to process the vitamin biotin in the normal way. Early symptoms of biotinidase deficiency generally Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:37:29 Biotinidase deficiency Biotinidase Biotin Newborn screening Multiple carboxylase deficiency Holocarboxylase synthetase deficiency Health Genetics Genetic genealogy
55	NATIONAL NEWBORN SCREENING REPORT[removed]Final Report: December, 2001 National Newborn Screening Report[removed] Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2002-01-24 11:36:38 Rare diseases Epidemiology Newborn screening Adrenal gland disorders Intersexuality Galactosemia Congenital adrenal hyperplasia Biotinidase deficiency Cystic fibrosis Health Medicine Pediatrics
56	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Rare diseases Epidemiology Newborn screening Biotinidase deficiency Biotinidase Immunoreactive trypsinogen Galactosemia Cystic fibrosis transmembrane conductance regulator Cystic fibrosis Health Pediatrics Medicine
57	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Genetics Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Biotinidase deficiency Biotinidase Galactosemia Biotin Congenital adrenal hyperplasia Health Medicine Pediatrics
58	Newborn Screening Fact Sheets Celia I. Kaye and and the Committee on Genetics Pediatrics 2006;118;[removed]DOI: [removed]peds[removed]This information is current as of September 6, 2006 Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-01-12 15:50:26 Adrenal gland disorders Intersexuality Rare diseases Deafness Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital adrenal hyperplasia Newborn screening Biotinidase deficiency Congenital hearing loss Health Medicine Pediatrics
59	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Epidemiology Newborn screening Pediatrics Inborn errors of carbohydrate metabolism Biotinidase deficiency Biotinidase Galactosemia Biotin C16 Health Genetics Medicine
60	National Newbor n Screening 2001 Incidence Repor t Tabulated incidence data for Newborn Screening Disorders organized by State and Genetics and Newborn Screening Regional Collaborative Groups National Newborn Screening Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-02-23 16:23:58 Mental retardation Epidemiology Newborn screening Medical specialties Biotinidase deficiency Medical genetics Galactosemia Phenylketonuria Association of Public Health Laboratories Medicine Health Pediatrics

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