Results 181 to 190 of about 7,513 (218)
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Lilis Supratman, Talita Savana, Lilis Supratman, Desti Herawati, Isrotun Ngesti Utami, Ilah Nurlaelah, Bayu Widiyanto, Ibni Annas ISBN: 978-634-4-2337-2 Tebal: ix + 232 hlm., 21 x 14 cm Juli 2025 Editor: Lilis Supratman Penata Letak: Diwantika Rachman Penata Sampul: Rehan Raharjo Penerbit PT. SIGMA LITERA GLOBAL Jl. Dr. Setia Budi No. 76 Rt. 02 Rw.
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2013
Craniosynostoses are premature fusions of one or more cranial sutures. They affect all cranial sutures and are the main symptom of many genetic syndromes. Syndromes connected with craniosynostosis are serious disorders associated with skeleton abnormalities, limb malformations or mental disability.
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Craniosynostoses are premature fusions of one or more cranial sutures. They affect all cranial sutures and are the main symptom of many genetic syndromes. Syndromes connected with craniosynostosis are serious disorders associated with skeleton abnormalities, limb malformations or mental disability.
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Genetika afektivnih poremećaja
2006Vjeruje se da su afektivni poremećaji uzrokovani većim brojem gena s malim efektom čija ekspresija ovisi o faktorima okoline Afektivni poremećaji spadaju u složene genske poremećaje, a to znači da se poremećaj ne može pripisati pojedinačnim dominantnim ili recesivnim genima u općoj populaciji.
Štrkalj-Ivezić, Slađana +6 more
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2007
U odlomku su opisane dosadašnje spoznaje o nasljednoj osnovi psihijatrijskih bolesti, metodologija genetičkih istraživanja, prikazan je pregled genskih polimorfizama koji se povezuju s pojavom različitih psihijatrijskih bolesti, te je opisano značenje farmakogenomike u psihijatriji.
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U odlomku su opisane dosadašnje spoznaje o nasljednoj osnovi psihijatrijskih bolesti, metodologija genetičkih istraživanja, prikazan je pregled genskih polimorfizama koji se povezuju s pojavom različitih psihijatrijskih bolesti, te je opisano značenje farmakogenomike u psihijatriji.
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2019
Hipofizės adenomos yra gėrybiniai priekinės hipofizės dalies augliai. Radiolginių ir autopsijų studijų duomenimis, hipofizės adenomos yra gana dažnos, nustatomos 15-20 proc. žmonių. Tai trečias pagal dažnį intrakranijinis auglys po meningiomų ir gliomų. Hipofizės adenomos 95 proc.
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Hipofizės adenomos yra gėrybiniai priekinės hipofizės dalies augliai. Radiolginių ir autopsijų studijų duomenimis, hipofizės adenomos yra gana dažnos, nustatomos 15-20 proc. žmonių. Tai trečias pagal dažnį intrakranijinis auglys po meningiomų ir gliomų. Hipofizės adenomos 95 proc.
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Miskonsepsi Materi Genetika tentang Ekspresi Gen
BIOEDUSAINS: Jurnal Pendidikan Biologi Dan Sains, 2020Tomi Hidayat
exaly
2018
Chromosome 21 is autosomal and acrocentric chromosome whose full or partial aneuploidy causes pathological changes in the carrier phenotype. Among the many types of aberrations, dominate standard trisomy 21, known as Down syndrome. This disorder also occurs as a result of duplication, deletion and translocation in the genome or as a result of the ...
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Chromosome 21 is autosomal and acrocentric chromosome whose full or partial aneuploidy causes pathological changes in the carrier phenotype. Among the many types of aberrations, dominate standard trisomy 21, known as Down syndrome. This disorder also occurs as a result of duplication, deletion and translocation in the genome or as a result of the ...
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Molekularna forenzična genetika
2009IZVOD IZ RECENZIJE Tekst obuhvata aktualne sadržaje koji su detaljno i zanimljivo prezentirani. Dosljedno elaborirajući moderan i inovativan pristup autori nas upoznaju sa osnovnim parametrima molekularne forenzične genetike, kako u sferi njenih znanstvenih temelja tako i u oblasti njene konkretne primjene.
Primorac, Dragan, Marjanović, Damir
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ALGORITMA EVOLUSI GENETIKA SEBAGAI FUNGSI OPTIMASI JARINGAN SARAF BUATAN
Device, 2021Muhamad Fuat Asnawi
exaly
2012
The most common form of monogenic diabetes is MODY (Maturity-Onset Diabetes of the Young). It ranks among genetic defects of the β cell. It is clinically heterogenous group of disorders characterised with non insulin-dependent diabetes mellitus with autosomal dominant inheritance and age at diagnosis up to 40 years.
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The most common form of monogenic diabetes is MODY (Maturity-Onset Diabetes of the Young). It ranks among genetic defects of the β cell. It is clinically heterogenous group of disorders characterised with non insulin-dependent diabetes mellitus with autosomal dominant inheritance and age at diagnosis up to 40 years.
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