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B Karaman

Showing results (11-20 of 35) with videos related to

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Journal of Neuroradiology = Journal De Neuroradiologie|April 7, 2015
Brain herniation with surrounding CSF into the skull or encepholecele?B Battal, S Hamcan, V Akgun, et al.
Clinical Radiology|June 1, 2014
Re: Role of diffusion-weighted MRI in differentiation of hepatic abscesses from non-infected fluid collectionsV Akgun, S Sari, B Battal, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2020
Prenatal Diagnosis of <i>a De Novo</i> Partial Trisomy 6q and Partial Monosomy 18p Associated with Cephalocele: A Case ReportA Karaman, B Karaman, A Çetinkaya, et al.
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|September 17, 2014
Osteoid osteoma radiofrequency ablationS Sari, S Celikkanat, K Kara, et al.
Prenatal Diagnosis|April 4, 2003
A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish familyB Karaman, B Wollnik, H Ermiş, et al.
Journal of Gastroenterology and Hepatology|March 3, 2005
Images of interest. Gastrointestinal: Abdominal neurofibromatosisB Karaman, C C Basekim, M Kantarci, et al.
Hereditas|October 7, 1998
An unusual translocation between 12tel and 14q11 in a large kindredS Palanduz, D Ustek, B Karaman, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)S Yakut, Z Cetin, C Sanhal, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGHS Yakut, Z Cetin, C Sanhal, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)Z Cetin, I Mendilcioglu, S Yakut, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal of Neuroradiology = Journal De Neuroradiologie|April 7, 2015
Brain herniation with surrounding CSF into the skull or encepholecele?B Battal, S Hamcan, V Akgun, et al.
Clinical Radiology|June 1, 2014
Re: Role of diffusion-weighted MRI in differentiation of hepatic abscesses from non-infected fluid collectionsV Akgun, S Sari, B Battal, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2020
Prenatal Diagnosis of <i>a De Novo</i> Partial Trisomy 6q and Partial Monosomy 18p Associated with Cephalocele: A Case ReportA Karaman, B Karaman, A Çetinkaya, et al.
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|September 17, 2014
Osteoid osteoma radiofrequency ablationS Sari, S Celikkanat, K Kara, et al.
Prenatal Diagnosis|April 4, 2003
A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish familyB Karaman, B Wollnik, H Ermiş, et al.
Journal of Gastroenterology and Hepatology|March 3, 2005
Images of interest. Gastrointestinal: Abdominal neurofibromatosisB Karaman, C C Basekim, M Kantarci, et al.
Hereditas|October 7, 1998
An unusual translocation between 12tel and 14q11 in a large kindredS Palanduz, D Ustek, B Karaman, et al.
Genetic Counseling (Geneva, Switzerland)|September 10, 2015
PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)S Yakut, Z Cetin, C Sanhal, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGHS Yakut, Z Cetin, C Sanhal, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)Z Cetin, I Mendilcioglu, S Yakut, et al.
Pageof 4