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Publications by DC Albert
PO-0827 Conotruncal Heart Defect in a Patient With Congenital Disorder of Glycosylation Type I
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
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Anesthetic Management of a Boy With Congenital Disorder of Glycosylation (CDG) I-X
International Journal of Clinical Medicine
Congenital Disorder of Glycosylation
MPDU1 Mutations Underlie a Novel Human Congenital Disorder of Glycosylation, Designated Type If
Journal of Clinical Investigation
Medicine
Novel Compound Heterozygous COG5 Mutations in a Chinese Male Patient With Severe Clinical Symptoms and Type�IIi Congenital Disorder of Glycosylation: A Case Report
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation
American Journal of Human Genetics
Genetics
Peter’s Type Ii Anomaly Associated With Congenital Heart Defect: Rare Case Report
Journal of Evidence Based Medicine and Healthcare
Conotruncal Heart Defect/Microphthalmia Syndrome: Delineation of an Autosomal Recessive Syndrome.
Journal of Medical Genetics
Genetics
A Case of Fatal Type I Congenital Disorders of Glycosylation (CDG I) Associated With Low Dehydrodolichol Diphosphate Synthase (DHDDS) Activity
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Congenital Disorders of Glycosylation. Part I. Defects of Protein N-Glycosylation.
Acta Biochimica Polonica
Biochemistry
Genetics
Molecular Biology
