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Mustafa Tekin

Showing results (131-140 of 235) with videos related to

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Pediatric Nephrology (Berlin, Germany)|July 2, 2013
High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUTBurcu Bulum, Z Birsin Ozçakar, Evren Ustüner, et al.
Clinical Genetics|August 22, 2019
Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing lossOscar Diaz-Horta, Guney Bademci, Suna Tokgoz-Yilmaz, et al.
Nursing Children and Young People|December 15, 2015
Prenatal maternal risk factors for infantile colicNazan Kaymaz, Şule Yıldırım, Naci Topaloğlu, et al.
Hormone Research in Paediatrics|November 25, 2015
Relationship between Abdominal Aortic Intima Media Thickness and Central Obesity in ChildrenHakan Aylanç, Nilüfer Aylanç, Şule Yıldırım, et al.
American Journal of Medical Genetics. Part A|March 29, 2023
H4C5 missense variant leads to a neurodevelopmental phenotype overlapping with Angelman syndromeNicholas Borja, Paulo Borjas-Mendoza, Stephanie Bivona, et al.
Journal of Orthopaedic Surgery and Research|March 22, 2026
Determinants of mortality following intertrochanteric fractures, comorbidities versus reduction quality: retrospective cohort studyBugra Kundakci, Talantbek Altoroev, Kaan Ali Dalkir, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 2006
Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patientsZ Birsin Ozçakar, F Başak Cengiz, Nilgün Cakar, et al.
The Laryngoscope|December 2, 2009
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontiaReinhard Ramsebner, Martin Ludwig, Thomas Parzefall, et al.
Molecular Cytogenetics|August 21, 2018
Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomaliesMeng Su, Paul J Benke, Guney Bademci, et al.
American Journal of Human Genetics|November 2, 2010
MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromesAsli Sirmaci, Tom Walsh, Hatice Akay, et al.
Pageof 24

Showing results (131-140 of 235) with videos related to

Sort By:
Pageof 24
Pediatric Nephrology (Berlin, Germany)|July 2, 2013
High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUTBurcu Bulum, Z Birsin Ozçakar, Evren Ustüner, et al.
Clinical Genetics|August 22, 2019
Novel variant p.E269K confirms causative role of PLS1 mutations in autosomal dominant hearing lossOscar Diaz-Horta, Guney Bademci, Suna Tokgoz-Yilmaz, et al.
Nursing Children and Young People|December 15, 2015
Prenatal maternal risk factors for infantile colicNazan Kaymaz, Şule Yıldırım, Naci Topaloğlu, et al.
Hormone Research in Paediatrics|November 25, 2015
Relationship between Abdominal Aortic Intima Media Thickness and Central Obesity in ChildrenHakan Aylanç, Nilüfer Aylanç, Şule Yıldırım, et al.
American Journal of Medical Genetics. Part A|March 29, 2023
H4C5 missense variant leads to a neurodevelopmental phenotype overlapping with Angelman syndromeNicholas Borja, Paulo Borjas-Mendoza, Stephanie Bivona, et al.
Journal of Orthopaedic Surgery and Research|March 22, 2026
Determinants of mortality following intertrochanteric fractures, comorbidities versus reduction quality: retrospective cohort studyBugra Kundakci, Talantbek Altoroev, Kaan Ali Dalkir, et al.
Pediatric Nephrology (Berlin, Germany)|July 1, 2006
Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patientsZ Birsin Ozçakar, F Başak Cengiz, Nilgün Cakar, et al.
The Laryngoscope|December 2, 2009
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontiaReinhard Ramsebner, Martin Ludwig, Thomas Parzefall, et al.
Molecular Cytogenetics|August 21, 2018
Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomaliesMeng Su, Paul J Benke, Guney Bademci, et al.
American Journal of Human Genetics|November 2, 2010
MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromesAsli Sirmaci, Tom Walsh, Hatice Akay, et al.
Pageof 24