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P F Giampietro

Showing results (11-20 of 21) with videos related to

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Molecular Syndromology|May 9, 2013
Clinical, genetic and environmental factors associated with congenital vertebral malformationsP F Giampietro, C L Raggio, R D Blank, et al.
American Journal of Medical Genetics|June 24, 1998
New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemiaP F Giampietro, A D Auerbach, E R Elias, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qterA L Wang, F X Arredondo-Vega, P F Giampietro, et al.
Pediatrics|June 1, 1993
The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia RegistryP F Giampietro, B Adler-Brecher, P C Verlander, et al.
Journal of Pediatric Orthopedics|November 30, 2000
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral densityT Do, P F Giampietro, S W Burke, et al.
Developmental Medicine and Child Neurology|December 1, 1992
Fanconi anemia: a model for genetic causes of abnormal brain developmentS G Pavlakis, C L Frissora, P F Giampietro, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 10, 2009
The role of cigarette smoking and statins in the development of postmenopausal osteoporosis: a pilot study utilizing the Marshfield Clinic Personalized Medicine CohortP F Giampietro, C McCarty, B Mukesh, et al.
American Journal of Medical Genetics|May 17, 1996
Fragile X syndrome in two siblings with major congenital malformationsP F Giampietro, B R Haas, E Lipper, et al.
Pediatrics|May 23, 2001
Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia RegistryM P Wajnrajch, J M Gertner, Z Huma, et al.
Clinical Genetics|October 7, 2005
An analysis of PAX1 in the development of vertebral malformationsP F Giampietro, C L Raggio, C E Reynolds, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Molecular Syndromology|May 9, 2013
Clinical, genetic and environmental factors associated with congenital vertebral malformationsP F Giampietro, C L Raggio, R D Blank, et al.
American Journal of Medical Genetics|June 24, 1998
New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemiaP F Giampietro, A D Auerbach, E R Elias, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1981
Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qterA L Wang, F X Arredondo-Vega, P F Giampietro, et al.
Pediatrics|June 1, 1993
The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia RegistryP F Giampietro, B Adler-Brecher, P C Verlander, et al.
Journal of Pediatric Orthopedics|November 30, 2000
The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral densityT Do, P F Giampietro, S W Burke, et al.
Developmental Medicine and Child Neurology|December 1, 1992
Fanconi anemia: a model for genetic causes of abnormal brain developmentS G Pavlakis, C L Frissora, P F Giampietro, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 10, 2009
The role of cigarette smoking and statins in the development of postmenopausal osteoporosis: a pilot study utilizing the Marshfield Clinic Personalized Medicine CohortP F Giampietro, C McCarty, B Mukesh, et al.
American Journal of Medical Genetics|May 17, 1996
Fragile X syndrome in two siblings with major congenital malformationsP F Giampietro, B R Haas, E Lipper, et al.
Pediatrics|May 23, 2001
Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia RegistryM P Wajnrajch, J M Gertner, Z Huma, et al.
Clinical Genetics|October 7, 2005
An analysis of PAX1 in the development of vertebral malformationsP F Giampietro, C L Raggio, C E Reynolds, et al.
Pageof 3