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T Mattina

Showing results (21-30 of 28) with videos related to

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American Journal of Medical Genetics|February 1, 1991
RFLP analysis in 5 Sicilian families with the fragile X syndromeV Romano, G Mascali, V Chiavetta, et al.
Nature|July 13, 1995
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2C Jones, L Penny, T Mattina, et al.
American Journal of Human Genetics|March 1, 1995
Clinical and molecular characterization of patients with distal 11q deletionsL A Penny, M Dell'Aquila, M C Jones, et al.
Journal of Medical Genetics|November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formationE Rossi, M Riegel, J Messa, et al.
Neurogenetics|October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)C D Coldren, Z Lai, P Shragg, et al.
Human Mutation|April 24, 2001
Nine novel APC mutations in Italian FAP patientsN Resta, A Stella, F Susca, et al.
Journal of Medical Genetics|September 26, 2007
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)M M Hagleitner, A Lankester, P Maraschio, et al.
Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
American Journal of Medical Genetics|February 1, 1991
RFLP analysis in 5 Sicilian families with the fragile X syndromeV Romano, G Mascali, V Chiavetta, et al.
Nature|July 13, 1995
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2C Jones, L Penny, T Mattina, et al.
American Journal of Human Genetics|March 1, 1995
Clinical and molecular characterization of patients with distal 11q deletionsL A Penny, M Dell'Aquila, M C Jones, et al.
Journal of Medical Genetics|November 17, 2007
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formationE Rossi, M Riegel, J Messa, et al.
Neurogenetics|October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)C D Coldren, Z Lai, P Shragg, et al.
Human Mutation|April 24, 2001
Nine novel APC mutations in Italian FAP patientsN Resta, A Stella, F Susca, et al.
Journal of Medical Genetics|September 26, 2007
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)M M Hagleitner, A Lankester, P Maraschio, et al.
Journal of Medical Genetics|September 4, 2007
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patientsM De Gregori, R Ciccone, P Magini, et al.
Pageof 3