golder-n-wilson documents

Zellweger syndrome: Diagnostic assays, syndrome delineation, and potential therapy
Documents Zellweger syndrome: Diagnostic assays, syndrome delineation, and potential therapy
Occurrence of holoprosencephaly in chromosome 13 disorders cannot be explained by duplication/deficiency of a single locus
Documents Occurrence of holoprosencephaly in chromosome 13 disorders cannot be explained by duplication/deficiency of a single locus
Glutaric aciduria type II: Review of the phenotype and report of an unusual glomerulopathy
Documents Glutaric aciduria type II: Review of the phenotype and report of an unusual glomerulopathy
Keratitis, hepatitis, ichthyosis, and deafness: Report and review of KID syndrome
Documents Keratitis, hepatitis, ichthyosis, and deafness: Report and review of KID syndrome
Index finger hyperphalangy and multiple anomalies: Catel-manzke syndrome?
Documents Index finger hyperphalangy and multiple anomalies: Catel-manzke syndrome?
Connective tissue and its heritable disorders: Molecular, genetic, and medical aspects. Peter M. Royce and Beat Steinmann, eds. New York: Wiley-Liss, 1993, 709 pp
Documents Connective tissue and its heritable disorders: Molecular, genetic, and medical aspects. Peter M. Royce and Beat Steinmann, eds. New York: Wiley-Liss, 1993, 709 pp
Coming together for blastogenesis
Documents Coming together for blastogenesis
Genomic imprinting: Summary of an NICHD conference
Documents Genomic imprinting: Summary of an NICHD conference
Book review
Documents Book review
A user's guide to the elements of standard morphologic terminology: Analysis and database
Documents A user's guide to the elements of standard morphologic terminology: Analysis and database
Mutational risks in females: genomic imprinting and maternal molecules
Documents Mutational risks in females: genomic imprinting and maternal molecules
Structure and variability of mammalian peroxisomal membrane proteins
Documents Structure and variability of mammalian peroxisomal membrane proteins
Structure-function relationships in the peroxisome: Implications for human disease
Documents Structure-function relationships in the peroxisome: Implications for human disease