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Gökhan Nalbant

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American Journal of Medical Genetics. Part A|September 27, 2021
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopodsSajid Malik, Gökhan Nalbant, Moqadsa Noreen, et al.
Clinical Genetics|July 30, 2019
FAM160B1 deficit associated with microcephaly, severe intellectual disability, ataxia, behavioral abnormalities and speech problemsRezan Nehir Mavioğlu, Bülent Kara, Gür Akansel, et al.
Journal of Medical Genetics|March 9, 2018
Homozygous <i>CHST11</i> mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactylyRana Muhammad Kamran Shabbir, Gökhan Nalbant, Nafees Ahmad, et al.
European Journal of Medical Genetics|March 1, 2021
CRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomaliesMine Koprulu, Rana Muhammad Kamran Shabbir, Qamar Zaman, et al.
Plos One|June 20, 2024
An intelligent algorithm for energy efficiency optimization in software-defined wireless sensor networks for 5G communicationsKemal Gökhan Nalbant, Suliman A Alsuhibany, Asma Hassan Alshehri, et al.
The Yale Journal of Biology and Medicine|October 2, 2023
A Recurrent Mutation in Growth Hormone Receptor (<i>GHR</i>) Gene Underlying Laron-type Dwarfism in a Pakistani FamilyRana Muhammad Kamran Shabbir, Gökhan Nalbant, Qamar Zaman, et al.
European Journal of Medical Genetics|April 24, 2020
Novel EDAR mutation in tooth agenesis and variable associated featuresSara Mumtaz, Gökhan Nalbant, Esra Yıldız Bölükbaşı, et al.
Plos One|July 17, 2024
An efficient algorithm for data transmission certainty in IIoT sensing network: A priority-based approachKemal Gökhan Nalbant, Sultan Almutairi, Asma Hassan Alshehri, et al.
The Yale Journal of Biology and Medicine|October 2, 2023
Homozygous Mutations in Thyroid Peroxidase (TPO) in Hypothyroidism with Intellectual Disability, Developmental Delay, and Hearing and Ocular Anomalies in Two Families: Severe Manifestation of Untreated TPO-deficiency Poses a Diagnostic DilemmaSyeda Farwa Naqvi, Esra Yıldız-Bölükbaşı, Muhammad Afzal, et al.
European Journal of Human Genetics : EJHG|June 8, 2022
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomaliesMine Koprulu, Muhammad Naeem, Gökhan Nalbant, et al.
Pageof 1

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

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|September 27, 2021
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopodsSajid Malik, Gökhan Nalbant, Moqadsa Noreen, et al.
Clinical Genetics|July 30, 2019
FAM160B1 deficit associated with microcephaly, severe intellectual disability, ataxia, behavioral abnormalities and speech problemsRezan Nehir Mavioğlu, Bülent Kara, Gür Akansel, et al.
Journal of Medical Genetics|March 9, 2018
Homozygous <i>CHST11</i> mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactylyRana Muhammad Kamran Shabbir, Gökhan Nalbant, Nafees Ahmad, et al.
European Journal of Medical Genetics|March 1, 2021
CRADD and USP44 mutations in intellectual disability, mild lissencephaly, brain atrophy, developmental delay, strabismus, behavioural problems and skeletal anomaliesMine Koprulu, Rana Muhammad Kamran Shabbir, Qamar Zaman, et al.
Plos One|June 20, 2024
An intelligent algorithm for energy efficiency optimization in software-defined wireless sensor networks for 5G communicationsKemal Gökhan Nalbant, Suliman A Alsuhibany, Asma Hassan Alshehri, et al.
The Yale Journal of Biology and Medicine|October 2, 2023
A Recurrent Mutation in Growth Hormone Receptor (<i>GHR</i>) Gene Underlying Laron-type Dwarfism in a Pakistani FamilyRana Muhammad Kamran Shabbir, Gökhan Nalbant, Qamar Zaman, et al.
European Journal of Medical Genetics|April 24, 2020
Novel EDAR mutation in tooth agenesis and variable associated featuresSara Mumtaz, Gökhan Nalbant, Esra Yıldız Bölükbaşı, et al.
Plos One|July 17, 2024
An efficient algorithm for data transmission certainty in IIoT sensing network: A priority-based approachKemal Gökhan Nalbant, Sultan Almutairi, Asma Hassan Alshehri, et al.
The Yale Journal of Biology and Medicine|October 2, 2023
Homozygous Mutations in Thyroid Peroxidase (TPO) in Hypothyroidism with Intellectual Disability, Developmental Delay, and Hearing and Ocular Anomalies in Two Families: Severe Manifestation of Untreated TPO-deficiency Poses a Diagnostic DilemmaSyeda Farwa Naqvi, Esra Yıldız-Bölükbaşı, Muhammad Afzal, et al.
European Journal of Human Genetics : EJHG|June 8, 2022
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomaliesMine Koprulu, Muhammad Naeem, Gökhan Nalbant, et al.
Pageof 1