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P F Giampietro

Showing results (1-10 of 21) with videos related to

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Analytical Biochemistry|May 1, 1983
Determination of delta-aminolevulinate dehydratase activity by a specific fluorometric coupled-enzyme assayP F Giampietro, R J Desnick
The New England Journal of Medicine|March 10, 1994
Fanconi's anemiaP F Giampietro, J G Davis, A D Auerbach
American Journal of Medical Genetics|March 30, 1999
Synteny-defined candidate genes for congenital and idiopathic scoliosisP F Giampietro, C L Raggio, R D Blank
Mayo Clinic Proceedings|August 14, 2001
Prevalence and patterns of presentation of genetic disorders in a pediatric emergency departmentP Kumar, J Radhakrishnan, M A Chowdhary, et al.
Lupus|August 31, 1999
A genomic approach to scoliosis pathogenesisR D Blank, C L Raggio, P F Giampietro, et al.
Personalized Medicine|May 24, 2018
Healthy People 2010 disease prevalence in the Marshfield Clinic Personalized Medicine Research Project cohort: opportunities for public health genomic researchC A McCarty, B N Mukesh, P F Giampietro, et al.
American Journal of Medical Genetics|January 10, 1997
Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry StudyP F Giampietro, P C Verlander, J G Davis, et al.
Blood|July 1, 1997
Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry studyA P Gillio, P C Verlander, S D Batish, et al.
Skeletal Radiology|April 1, 1996
Congenital fusion of the fourth and fifth metacarpals associated with primary gonadal failureW D Donovan, P W Brill, P Winchester, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 6, 2005
Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndromeP F Giampietro, D B Schowalter, S Merchant, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Analytical Biochemistry|May 1, 1983
Determination of delta-aminolevulinate dehydratase activity by a specific fluorometric coupled-enzyme assayP F Giampietro, R J Desnick
The New England Journal of Medicine|March 10, 1994
Fanconi's anemiaP F Giampietro, J G Davis, A D Auerbach
American Journal of Medical Genetics|March 30, 1999
Synteny-defined candidate genes for congenital and idiopathic scoliosisP F Giampietro, C L Raggio, R D Blank
Mayo Clinic Proceedings|August 14, 2001
Prevalence and patterns of presentation of genetic disorders in a pediatric emergency departmentP Kumar, J Radhakrishnan, M A Chowdhary, et al.
Lupus|August 31, 1999
A genomic approach to scoliosis pathogenesisR D Blank, C L Raggio, P F Giampietro, et al.
Personalized Medicine|May 24, 2018
Healthy People 2010 disease prevalence in the Marshfield Clinic Personalized Medicine Research Project cohort: opportunities for public health genomic researchC A McCarty, B N Mukesh, P F Giampietro, et al.
American Journal of Medical Genetics|January 10, 1997
Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry StudyP F Giampietro, P C Verlander, J G Davis, et al.
Blood|July 1, 1997
Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry studyA P Gillio, P C Verlander, S D Batish, et al.
Skeletal Radiology|April 1, 1996
Congenital fusion of the fourth and fifth metacarpals associated with primary gonadal failureW D Donovan, P W Brill, P Winchester, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 6, 2005
Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndromeP F Giampietro, D B Schowalter, S Merchant, et al.
Pageof 3