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F Gurrieri

Showing results (31-40 of 37) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.
Nature Genetics|March 1, 1993
Physical mapping of the holoprosencephaly critical region on chromosome 7q36F Gurrieri, B J Trask, G van den Engh, et al.
American Journal of Medical Genetics|May 17, 1996
Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regionsG Sebastio, L Perone, V Guzzetta, et al.
American Journal of Medical Genetics|April 24, 1996
A split hand-split foot (SHFM3) gene is located at 10q24-->25F Gurrieri, P Prinos, D Tackels, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literatureL Garavelli, M Zollino, P Cerruti Mainardi, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Proceedings of the National Academy of Sciences of the United States of America|August 16, 1994
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneityM Muenke, F Gurrieri, C Bay, et al.
Nature Genetics|March 1, 1993
Physical mapping of the holoprosencephaly critical region on chromosome 7q36F Gurrieri, B J Trask, G van den Engh, et al.
American Journal of Medical Genetics|May 17, 1996
Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21)(p16.3;q22.1): relevance to the Wolf-Hirschhorn and Down syndrome critical regionsG Sebastio, L Perone, V Guzzetta, et al.
American Journal of Medical Genetics|April 24, 1996
A split hand-split foot (SHFM3) gene is located at 10q24-->25F Gurrieri, P Prinos, D Tackels, et al.
Neuropediatrics|December 7, 2007
Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new caseL Garavelli, E Guareschi, S Errico, et al.
American Journal of Human Genetics|July 20, 2001
p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.
American Journal of Medical Genetics. Part A|February 14, 2009
Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literatureL Garavelli, M Zollino, P Cerruti Mainardi, et al.
Pageof 4