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G Hoganson

Showing results (11-20 of 17) with videos related to

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Clinical Genetics|June 1, 1989
A pseudoisochromosome 18q and an isodicentric chromosome 18C Floore, A Robertson, I Samuel, et al.
Pediatrics|December 1, 1984
Biopterin synthesis defects: problems in diagnosisG Hoganson, S Berlow, S Kaufman, et al.
Genomics|August 22, 2000
Canine heparan sulfate sulfamidase and the molecular pathology underlying Sanfilippo syndrome type A in DachshundsE L Aronovich, K P Carmichael, H Morizono, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
Phenylketonuria in adulthood: a collaborative studyR Koch, B Burton, G Hoganson, et al.
Neurology|July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patientsE Pegoraro, H Marks, C A Garcia, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Clinical Genetics|June 1, 1989
A pseudoisochromosome 18q and an isodicentric chromosome 18C Floore, A Robertson, I Samuel, et al.
Pediatrics|December 1, 1984
Biopterin synthesis defects: problems in diagnosisG Hoganson, S Berlow, S Kaufman, et al.
Genomics|August 22, 2000
Canine heparan sulfate sulfamidase and the molecular pathology underlying Sanfilippo syndrome type A in DachshundsE L Aronovich, K P Carmichael, H Morizono, et al.
Annals of Neurology|October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndromeS DiMauro, S Servidei, M Zeviani, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
Phenylketonuria in adulthood: a collaborative studyR Koch, B Burton, G Hoganson, et al.
Neurology|July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patientsE Pegoraro, H Marks, C A Garcia, et al.
Pageof 2