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T Tos

Showing results (1-10 of 16) with videos related to

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Ugeskrift for Laeger|October 23, 2001
[Surgical treatment of sequelae after facial paralysis]T Tos, C Krag
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
A boy with Weyers-like ulnar ray/oligodactyly reduction limb defects and split hand malformation: case reportT Tos, A Karaman, D Gül
Genetic Counseling (Geneva, Switzerland)|February 28, 2018
A Rare Case of Hanhart Syndrome with Mild Developmental DelayG Gulec Ceylan, T Tos, E Sari
Genetic Counseling (Geneva, Switzerland)|August 19, 2011
A rare case of monosomy 18p: translocation between chromosomes 18 and 21T Tos, A Karaman, Z Aycan, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patientsT Tos, A Karaman, A Aksoy, et al.
Annals of the Rheumatic Diseases|July 16, 2003
Association of sister chromatid exchange frequencies in patients with ankylosing spondylitis with and without HLA-B27M Ikbal, N Ezirmik, T Tos, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
A case of otocephaly with anencephaly and meningomyeloceleT Tos, S Ceylaner, S Senel, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A familial case of Coffin-Lowry syndrome caused by RPS6KA3 C.898C>T mutation associated with multiple abnormal brain imaging findingsT Tos, M Y Alp, A Aksoy, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 2014
A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndromeP Zorlu, A S Eksioglu, M Ozkan, et al.
Genetic Counseling (Geneva, Switzerland)|February 5, 2011
A case of lower mesodermal defects sequenceT Tos, S Aktas, M Ikbal, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Ugeskrift for Laeger|October 23, 2001
[Surgical treatment of sequelae after facial paralysis]T Tos, C Krag
Genetic Counseling (Geneva, Switzerland)|October 28, 2011
A boy with Weyers-like ulnar ray/oligodactyly reduction limb defects and split hand malformation: case reportT Tos, A Karaman, D Gül
Genetic Counseling (Geneva, Switzerland)|February 28, 2018
A Rare Case of Hanhart Syndrome with Mild Developmental DelayG Gulec Ceylan, T Tos, E Sari
Genetic Counseling (Geneva, Switzerland)|August 19, 2011
A rare case of monosomy 18p: translocation between chromosomes 18 and 21T Tos, A Karaman, Z Aycan, et al.
Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patientsT Tos, A Karaman, A Aksoy, et al.
Annals of the Rheumatic Diseases|July 16, 2003
Association of sister chromatid exchange frequencies in patients with ankylosing spondylitis with and without HLA-B27M Ikbal, N Ezirmik, T Tos, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
A case of otocephaly with anencephaly and meningomyeloceleT Tos, S Ceylaner, S Senel, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A familial case of Coffin-Lowry syndrome caused by RPS6KA3 C.898C>T mutation associated with multiple abnormal brain imaging findingsT Tos, M Y Alp, A Aksoy, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 2014
A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndromeP Zorlu, A S Eksioglu, M Ozkan, et al.
Genetic Counseling (Geneva, Switzerland)|February 5, 2011
A case of lower mesodermal defects sequenceT Tos, S Aktas, M Ikbal, et al.
Pageof 2