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The Turkish Journal of Pediatrics
|
November 28, 2015
Association between teething and independent walking in healthy children
Nazan Kaymaz, Şule Yıldırım, Sibel Cevizci, et al.
Clinical Dysmorphology
|
June 7, 2007
A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy
Tümay Doğancı, Berrin E Yüksel Konuk, Nursel Alpan, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
22q11.2q13 duplication including SOX10 causes sex-reversal and peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease
Nadia Falah, Jennifer E Posey, Willa Thorson, et al.
European Journal of Human Genetics : EJHG
|
April 12, 2021
Confirmation of COL4A6 variants in X-linked nonsyndromic hearing loss and its clinical implications
Alexander O'Brien, Wen Yih Aw, Hui Yi Tee, et al.
Injury
|
December 3, 2024
Can trauma scores predict the length of hospital stay of patients with fractures after earthquake-related blunt injury?
Akif Mirioğlu, Veli Can Kıran, Kaan Ali Dalkir, et al.
Rheumatology International
|
March 24, 2009
Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy
Berrin Yüksel-Konuk, Aslı Sırmacı, Gülen Ece Ayten, et al.
American Journal of Human Genetics
|
July 29, 2008
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart
Kathleen S Arnos, Katherine O Welch, Mustafa Tekin, et al.
The Journal of Biological Chemistry
|
January 23, 2003
Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrix
Wayne A Cabral, Marianna V Mertts, Elena Makareeva, et al.
Turk Pediatri Arsivi
|
October 25, 2017
Research of genetic bases of hereditary non-syndromic hearing loss
Aslı Subaşıoğlu, Duygu Duman, Aslı Sırmacı, et al.
Journal of Orthopaedic Surgery and Research
|
July 27, 2023
6 February 2023, orthopedic experience in Kahramanmaraş earthquake and surgical decision in patients with crush syndrome
Bugra Kundakci, Akif Mirioglu, Mustafa Tekin, et al.
Page
of 24
Search research articles
Search
Showing results (111-120 of 235) with videos related to
Sort By:
Page
of 24
The Turkish Journal of Pediatrics
|
November 28, 2015
Association between teething and independent walking in healthy children
Nazan Kaymaz, Şule Yıldırım, Sibel Cevizci, et al.
Clinical Dysmorphology
|
June 7, 2007
A novel mutation in TRIM37 is associated with mulibrey nanism in a Turkish boy
Tümay Doğancı, Berrin E Yüksel Konuk, Nursel Alpan, et al.
American Journal of Medical Genetics. Part A
|
March 23, 2017
22q11.2q13 duplication including SOX10 causes sex-reversal and peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease
Nadia Falah, Jennifer E Posey, Willa Thorson, et al.
European Journal of Human Genetics : EJHG
|
April 12, 2021
Confirmation of COL4A6 variants in X-linked nonsyndromic hearing loss and its clinical implications
Alexander O'Brien, Wen Yih Aw, Hui Yi Tee, et al.
Injury
|
December 3, 2024
Can trauma scores predict the length of hospital stay of patients with fractures after earthquake-related blunt injury?
Akif Mirioğlu, Veli Can Kıran, Kaan Ali Dalkir, et al.
Rheumatology International
|
March 24, 2009
Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy
Berrin Yüksel-Konuk, Aslı Sırmacı, Gülen Ece Ayten, et al.
American Journal of Human Genetics
|
July 29, 2008
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart
Kathleen S Arnos, Katherine O Welch, Mustafa Tekin, et al.
The Journal of Biological Chemistry
|
January 23, 2003
Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrix
Wayne A Cabral, Marianna V Mertts, Elena Makareeva, et al.
Turk Pediatri Arsivi
|
October 25, 2017
Research of genetic bases of hereditary non-syndromic hearing loss
Aslı Subaşıoğlu, Duygu Duman, Aslı Sırmacı, et al.
Journal of Orthopaedic Surgery and Research
|
July 27, 2023
6 February 2023, orthopedic experience in Kahramanmaraş earthquake and surgical decision in patients with crush syndrome
Bugra Kundakci, Akif Mirioglu, Mustafa Tekin, et al.
Page
of 24