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Hunter syndrome
An Overview of Lesch-Nyhan Syndrome
(Hunter Syndrome) Complicated by Autoimmune Hemolytic Anemia
Mini-Review on “Molecular Diagnosis of 65 Families With
Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment
Megalencephaly and Macrocephaly
Newborn Screening for Mucopolysaccharidosis Type II in Illinois: an Update
X-Linked Diseases: Susceptible Females
Expression of Two X-Linked Genes in Human Hair Follicles of Double Heterozygotes (Lesch-Nyhan Syndrome/Gene Inactivation/Lyon Hypothesis) JOSEPH L
Assessment of Activity of Daily Life in Mucopolysaccharidosis Type II Patients with Hematopoietic Stem Cell Transplantation
Inherited Metabolic Diseases and Autism
Subject Index Proc
Autism Spectrum Disorder in a Child with Hunter Syndrome
Carrier of Hunter Disease J Med Genet: First Published As 10.1136/Jmg.34.2.137 on 1 February 1997
X-Chromosome Inactivation and Its Implications for Human Disease
Guidelines for Diagnosis and Treatment of Hunter Syndrome for Clinicians in Latin America
Beacon Carrier Screening Detecting 400+ Conditions
UC Irvine UC Irvine Previously Published Works
Clinical, Biochemical and Molecular Characteristics of Filipino Patients with Mucopolysaccharidosis Type II - Hunter Syndrome Mary Anne D
Top View
Hunter Syndrome
Mucopolysaccharidosis Type II (Hunter Syndrome): a Clinical Review and Recommendations for Treatment in the Era of Enzyme Replacement Therapy
Further Evidence Localising the Gene for Hunter's Long
How Including Patient Voices in Clinical Trial Design Can Deliver Many Bene;Ts
Recent Advances in Ophthalmic Genetics Genetic Counselling
Severe Phenotype in MPS II Patients Associated with a Large Deletion
Molecular Analyses in Families with Hunter Syndrome Indicate Unequal
Hunter's Syndrome and Oral Manifestations
What's New in Newborn Screening?
Expanded Carrier Screening
Iduronate Sulfatase Activity in Serum, Lymphocytes, and Fibroblasts-Simplified Diagnosis of the Hunter Syndrome
Mucopolysaccharidosis Type II
Hunter Syndrome/MPS II – FDA-Requested Listening Session February 4, 2020 Objectives of Session
Diagnosis of Inherited Metabolic Disorders Affecting the Nervous System
Huntersyndrome.Info to Learn More
Seven Additional Newborn Screening Disorders Coming to NJ: Are You Ready?
Prenatal Diagnosis and Genetic Counselling
He A-Z Reference Book of Syndromes and Inherited Disorders the A-Z Reference Book of Syndromes and Inherited Disorders
Elaprase (Idursulfase) C2720-A
Hunter Syndrome Caregiver Guide
Download The
Mucopolysaccharidosis Type II
Developmental Disabilities Handbook
PGD and Establishing a Hunter (46, XX) Stem Cell Line
Expanded Carrier Screen Gene List (By Gene)
January 4, 2020 the Honorable Frank Pallone Chairman Committee On
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Fetal Examination/Genetic Evaluation Information and Instructions
Deletion Xq27.3Q28 in Female Patient with Global Developmental Delays
Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions
Gene Therapy for Pediatric Diseases
Behaviour in Mucopolysaccharide Disorders
Cell and Gene Therapies for Mucopolysaccharidoses: Base Editing and Therapeutic Delivery to the CNS
Hunter Syndrome
Hunter's Syndrome: Description and Educational Considerations. PUB DATE 1999-00-00 NOTE 15P
Optic Canal Narrowing in Hunter Syndrome (Mucopolysaccharidosis II)
Mucopolysaccharidosis Type II: European Recommendations for The
The Impact of Hunter Syndrome (Mucopolysaccharidosis Type
I-DSD 2017 Poster Presentations
Molecular Genetic Defect Underlying A-L-Lduronidase Pseudodeficiency Elena L
Dosage Compensation in Females with X-Linked Metabolic Disorders
Hunter Syndrome): Results from a Systematic Evidence Review
Invitae Carrier Screening (Continued)
Hunter Syndrome a Rare Genetic Disease
Inherited Disease Screening
Ion Ampliseq™ Inherited Disease Panel Target Gene List
Established Conditions List
Gene Therapy for Inherited Muscle Diseases: Where Genetics Meets Rehabilitation Medicine
17 X Chromosome Rearrangements
Metabolic Correction and Cross-Correction Of
Institute of Anatomy and Biology, Philadelphia, Pennsylvania. Fusion
Blueprint Genetics Lysosomal Disorders And
Mendelian Disorders Among Jews