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Cancer Prevention Research (Philadelphia, Pa.)
|
February 16, 2024
Triple Primary Cancers: An Analysis of Genetic and Environmental Factors
Nicholas A Borja, Rachel Silva-Smith, Carmen Calfa, et al.
Acta Orthopaedica Et Traumatologica Turcica
|
March 13, 2016
Anatomic compatibility of femoral intramedullary implants: a cadaveric study
Ömer Sunkar Biçer, Gazi Huri, Mustafa Tekin, et al.
American Journal of Medical Genetics. Part A
|
January 7, 2022
Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant
Lé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
Journal of Perianesthesia Nursing : Official Journal of the American Society of Perianesthesia Nurses
|
July 31, 2025
4-7-8 Breathing Techniques Make It Possible to Reduce Pain Associated With Total Knee Arthroplasty: A New Technique in Respiratory Exercises
Zehra Eskimez, Alev Keskin, Ece Kurt, et al.
Acta Orthopaedica Et Traumatologica Turcica
|
April 13, 2022
Clinical and radiological outcomes of Salter versus Pemberton osteotomies in the management of developmental dysplasia of the hip: A retrospective comparative study
Akif Mirioğlu, Ömer Sunkar Biçer, Mustafa Tekin, et al.
Plos One
|
November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
Tahir Atik, Huseyin Onay, Ayca Aykut, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 2009
Modulation of Fgf3 dosage in mouse and men mirrors evolution of mammalian dentition
Cyril Charles, Vincent Lazzari, Paul Tafforeau, et al.
Medical Journal of the Islamic Republic of Iran
|
June 3, 2015
Protective role of Proanthocyanidin in experimental ovarian torsion
Şule Yıldırım, Naci Topaloğlu, Mustafa Tekin, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2004
The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype
Mustafa Tekin, Asli Kavaz, Merih Berberoğlu, et al.
European Journal of Pediatrics
|
April 17, 2014
Novel adenosine deaminase 2 mutations in a child with a fatal vasculopathy
Nisha Garg, Ozgur Kasapcopur, Joseph Foster, et al.
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of 24
Search research articles
Search
Showing results (51-60 of 235) with videos related to
Sort By:
Page
of 24
Cancer Prevention Research (Philadelphia, Pa.)
|
February 16, 2024
Triple Primary Cancers: An Analysis of Genetic and Environmental Factors
Nicholas A Borja, Rachel Silva-Smith, Carmen Calfa, et al.
Acta Orthopaedica Et Traumatologica Turcica
|
March 13, 2016
Anatomic compatibility of femoral intramedullary implants: a cadaveric study
Ömer Sunkar Biçer, Gazi Huri, Mustafa Tekin, et al.
American Journal of Medical Genetics. Part A
|
January 7, 2022
Bilateral choanal stenosis in auriculocondylar syndrome caused by a PLCB4 variant
Lé Shon Peart, Joanna Gonzalez, Stephanie Bivona, et al.
Journal of Perianesthesia Nursing : Official Journal of the American Society of Perianesthesia Nurses
|
July 31, 2025
4-7-8 Breathing Techniques Make It Possible to Reduce Pain Associated With Total Knee Arthroplasty: A New Technique in Respiratory Exercises
Zehra Eskimez, Alev Keskin, Ece Kurt, et al.
Acta Orthopaedica Et Traumatologica Turcica
|
April 13, 2022
Clinical and radiological outcomes of Salter versus Pemberton osteotomies in the management of developmental dysplasia of the hip: A retrospective comparative study
Akif Mirioğlu, Ömer Sunkar Biçer, Mustafa Tekin, et al.
Plos One
|
November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
Tahir Atik, Huseyin Onay, Ayca Aykut, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 2009
Modulation of Fgf3 dosage in mouse and men mirrors evolution of mammalian dentition
Cyril Charles, Vincent Lazzari, Paul Tafforeau, et al.
Medical Journal of the Islamic Republic of Iran
|
June 3, 2015
Protective role of Proanthocyanidin in experimental ovarian torsion
Şule Yıldırım, Naci Topaloğlu, Mustafa Tekin, et al.
American Journal of Medical Genetics. Part A
|
September 21, 2004
The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype
Mustafa Tekin, Asli Kavaz, Merih Berberoğlu, et al.
European Journal of Pediatrics
|
April 17, 2014
Novel adenosine deaminase 2 mutations in a child with a fatal vasculopathy
Nisha Garg, Ozgur Kasapcopur, Joseph Foster, et al.
Page
of 24