Prader–Willi syndrome and Angelman syndrome
Cited by (336)
Items 301–336 of 336
- Molecules and CellsScott F. Stoltenberg · 2022 · Cambridge University Press eBooks
- GenesScott F. Stoltenberg · 2022 · Cambridge University Press eBooks
- Neurodevelopmental Disorders: Epigenetic Implications and Potential Analysis MethodsRwik Sen · 2022 · Nutritional neurosciences
- Angelman/Prader-Willi SyndromesNicholas M. DiLullo, Abha R. Gupta · 2021 · Springer eBooks
- CONVULSÕES FEBRIS: PERSPECTIVAS HISTÓRICA E FUTURA À LUZ DA GENÉTICAMarcos Manoel Honorato, Adriele Feitosa Ribeiro, Susan Karolayne Silva Pimentel, Sandro Murilo Moreira de Lima, Jonata Ribeiro de Sousa, Renata Carvalho Cremaschi, Fernando Morgadinho Santos Coelho · 2021
- Angelman SyndromeHarold Chen · 2017 · Springer eBooks
- COMO MENDEL SE INTERESSOU PELA HERANÇA DAS CARACTERÍSTICAS?Luiz Augusto Salles das Neves, Raquel Stefanello, Renata Smith Avinio, Kelen Haygert Lencina · 2021
- A PREDISPOSIÇÃO GENÉTICA À DIABETES MELLITUS TIPO 2: UMA REVISÃO DA LITERATURAÍtalo Caio Lopes Jucá, José Hélder da Costa Vasconcelos, Lara Maria Alves de Carvalho, Maria Cecília Queiroga dos Santos, Sara da Rocha Silva, Ana Janaína Jeanine Martins de Lemos Jordão, Cristina Ruan Ferreira de Araújo · 2021
- David HaigManus M. Patten · 2018 · Springer eBooks
- ATUALIZAÇÕES DA NANOMEDICINA NO TRATAMENTO E DIAGNÓSTICO DE PACIENTES COM CANCERLucas Dalvi Armond Rezende, Aurélio Alberto Guizolpho, Luana da Silva Ferreira, Maira Dorighetto Ardisson, Anna Carolina Dockhorn de Menezes Carvalho Costa, Daniel Altoé Sossai, Maria Eduarda Morais Hibner Amaral, Pietra Zava Lorencini, Nathalia Oliveira Brunelli, Karolini Zuqui Nunes · 2021
- DOENÇA DE LAFORA: UMA REVISÃO SISTEMÁTICABarbara Novais Prado Machado · 2021
- SÍNDROME DE LI-FRAUMENI, TESTES GENÉTICOS E PERFIL GENÉTICO NO BRASIL.Deborah Ribeiro Nascimento, Gabriel de Sousa Andrade, Fernanda Meneses Monteiro, Isabella Gonçalves Oliveira, Ana Clara Martins Quirino, Igor Ribeiro Nascimento, Liane de Rosso Giuliani · 2021
- David HaigManus M. Patten · 2021 · Springer eBooks
- EDITH REBECCA SAUNDERS E A HEREDITARIEDADE NO FINAL DO SÉCULO XIXLuiz Augusto Salles das Neves, Raquel Stefanello, Renata Smith Avinio, Kelen Haygert Lencina · 2021
- Angelman Syndrome2012 · Springer eBooks
- Genetic etiologies of autism: Unpacking pathogenic mechanisms and characteristicsCaitlin M. Hudac, Nicole R. Friedman, Tychele N. Turner · 2022 · Elsevier eBooks
- Clinical Utility and Reporting of Absence of Heterozygosity in Chromosomal Microarray AnalysisKyoung Bo Kim, Jung‐Sook Ha · 2023 · Laboratory Medicine Online
- Understanding Prader-Will SyndromeOlubukola Christianah Dada, Adedayo Adesokan · 2023 · Advances in educational technologies and instructional design book series
- Therapeutic approaches to imprinting diseasesHela Sassi, Léa Guerrini‐Rousseau, Jacques Grill, Étienne Rouleau · 2023 · Elsevier eBooks
- Patterns of InheritanceBruce R Korf MD, PhD, Mira Irons · 2013 · Wiley eBooks
- Single-Gene AbnormalitiesSarah McKeown Ruggiero, Ingo Helbig · 2025 · Elsevier eBooks
- Gastrointestinal manifestations in Angelman syndrome with accompanying epilepsy: a pediatric case reportKamil Aleksander Sobieszek, Patrycja Idzik · 2025 · Egyptian Pediatric Association Gazette
- Additional file 1 of A case of an Angelman-syndrome caused by an intragenic duplication of UBE3A uncovered by adaptive nanopore sequencingLaura Holthöfer, Stefan Diederich, Verena Haug, Lioba Lehmann, Charlotte Hewel, Paul, Norbert W., Schweiger, Susann, Susanne Gerber, Matthias Linke · 2024 · Figshare
- Additional file 1 of Cortical and subcortical morphological alteration in Angelman syndromeDu, Xiaonan, Wei, Lei, Baofeng Yang, Long, Shasha, Wang, Ji, Sun, Aiqi, Jiang, Yonghui, Qiao, Zhongwei, Wang, He, Yi Wang · 2024 · Figshare
- Examination of the Chromatin Structure of Xlr3b Using the Chromosome Conformation Capture AssaySarah E. Conderino · 2012 · OpenCommons - UConn (University of Connecticut)
- Neonatal Bradypnea as an Under-Recognized Manifestation of Prader-Willi Syndrome: A Case ReportAnkit Ranjan, Shams Karim, Jeoffrey Jay Valentin, Sofia Fakih · 2026 · Cureus
- Identification et caractérisation de la fonction d’un réseau de gènes soumis à empreinteBrendan Evano · 2012 · theses.fr (ABES)
- Rôle de la protéine Bcd1p/BCD1 dans les étapes précoces de la biogenèse des snoRNP à boîtes C/D eucaryotesArnaud Paul · 2018 · theses.fr (ABES)
- Vers l'identification des facteurs impliqués dans la régulation concertée des gènes soumis à empreinte dans le cerveauJil Cercy · 2019 · theses.fr (ABES)
- Nouvel aperçu des partenaires moléculaires des snoRNP à boîtes C/D et des fonctions biologiques associéesLaeya Baldini · 2021 · theses.fr (ABES)
- Diversité, complexité et sévérité du handicap dans le syndrome de Prader-Willi : comprendre les particularités pour prévenir le surhandicap. Études réalisées à partir de la base de données de patients pédiatriques du Centre de référenceDibia Liz Pacoricona Alfaro · 2021 · theses.fr (ABES)
- Nadir Hastalıkların Klinik Sistem Temelli Sınıflandırılması: Modern Moleküler Biyoloji, Sistem Biyolojisi ve Translasyonel Tıp PerspektifleriNaciye Selcen Bayramcı, Rümeysa Demirkaya · 2026 · Özgür Yayınları eBooks
- Handle with care: packaging the oocyte epigenome for the next generationChloe A Edwards-Lee, Ellen G. Jarred, Patrick S. Western · 2026 · Reproduction Fertility and Development
- Environmental EpigeneticsBs Vaanrhaangh Anal · 2026 · Springer eBooks
- Current Status of Induced Pluripotent Stem CellsThach‐Vu Ho, Grace E. Asuelime, Wendong Li, Yanhong Shi · 2011 · Humana Press eBooks
- Genetyczne przyczyny upośledzenia umysłowego, z którymi neurolog może spotkać się w codziennej praktyceKarol Jastrzębski, Magdalena Justyna Kacperska, Tadeusz Pietras, Maciej Radek · 2013 · DOAJ (DOAJ: Directory of Open Access Journals)