Artykuły w czasopismach na temat „Genetic disorders in children”
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Ćirić, Sanela. "DIFFERENCES IN PARENTS' ATTITUDES TOWARDS THE CAUSES OF NEURODEVELOPMENTAL DISORDERS". Multidisciplinarni Pristupi u Edukaciji i Rehabilitaciji 6, nr 7 (15.08.2024): 161–70. http://dx.doi.org/10.59519/mper6115.
Pełny tekst źródłaFisch, Gene S., Nancy Carpenter, Patricia N. Howard-Peebles, Jeanette J. A. Holden, Jack Tarleton, Richard Simensen i Agatino Battaglia. "Developmental Trajectories in Syndromes With Intellectual Disability, With a Focus on Wolf-Hirschhorn and Its Cognitive–Behavioral Profile". American Journal on Intellectual and Developmental Disabilities 117, nr 2 (1.02.2012): 167–79. http://dx.doi.org/10.1352/1944-7558-117.2.167.
Pełny tekst źródłaLashwood, Alison. "Preimplantation genetic diagnosis to prevent genetic disorders in children". British Journal of Nursing 14, nr 2 (styczeń 2005): 64–70. http://dx.doi.org/10.12968/bjon.2005.14.2.17433.
Pełny tekst źródłaBarrie, Alpha-Umaru. "Youth perspectives on genetic inheritance, carrier status and disclosure". Journal of Haemophilia Practice 3, nr 2 (1.07.2016): 21–28. http://dx.doi.org/10.17225/jhp00077.
Pełny tekst źródłaRudin, I. V. "SPEECH DISORDERS OF GENETIC ORIGIN IN TEACHING PRACTICE". Education & Pedagogy Journal, nr 1(1) (6.07.2021): 56–63. http://dx.doi.org/10.23951/2782-2575-2021-1-56-63.
Pełny tekst źródłaMueller, Sven C., Pamela Ng, Ninet Sinaii, Ellen W. Leschek, Liza Green-Golan, Carol VanRyzin, Monique Ernst i Deborah P. Merke. "Psychiatric characterization of children with genetic causes of hyperandrogenism". European Journal of Endocrinology 163, nr 5 (listopad 2010): 801–10. http://dx.doi.org/10.1530/eje-10-0693.
Pełny tekst źródłaZhestkova, M. A., i D. Yu Ovsyannikov. "GENETIC DISORDERS OF SURFACTANT PROTEINS". Pediatria. Journal named after G.N. Speransky 100, nr 5 (11.10.2021): 82–89. http://dx.doi.org/10.24110/0031-403x-2021-100-5-82-89.
Pełny tekst źródłaYou, Haizhen, Junyao Shi, Fangfang Huang, Zhiyun Wei, Gary Jones, Wenchong Du i Jing Hua. "Advances in Genetics and Epigenetics of Developmental Coordination Disorder in Children". Brain Sciences 13, nr 6 (11.06.2023): 940. http://dx.doi.org/10.3390/brainsci13060940.
Pełny tekst źródłaPletcher, Beth A., i Nelson L. Turcios. "Pulmonary Manifestations of Genetic Disorders in Children". Pediatric Clinics of North America 68, nr 1 (luty 2021): 1–24. http://dx.doi.org/10.1016/j.pcl.2020.09.010.
Pełny tekst źródłaClauss, Sarah B., i Peter O. Kwiterovich. "Genetic disorders of lipoprotein transport in children". Progress in Pediatric Cardiology 17, nr 2 (wrzesień 2003): 123–33. http://dx.doi.org/10.1016/s1058-9813(03)00049-3.
Pełny tekst źródłaMorozova, E. A., M. V. Belousova, D. V. Morozov, D. I. Gabelko i V. V. Bogolyubova. "Genetic aspects of speech disorders in children". Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 123, nr 9 (2023): 87. http://dx.doi.org/10.17116/jnevro202312309287.
Pełny tekst źródłaFrans, E. M., P. Lichtenstein, C. M. Hultman i R. Kuja-Halkola. "Age at fatherhood: heritability and associations with psychiatric disorders". Psychological Medicine 46, nr 14 (12.08.2016): 2981–88. http://dx.doi.org/10.1017/s0033291716001744.
Pełny tekst źródłaFelsenfeld, Susan, i Robert Plomin. "Epidemiological and Offspring Analyses of Developmental Speech Disorders Using Data From the Colorado Adoption Project". Journal of Speech, Language, and Hearing Research 40, nr 4 (sierpień 1997): 778–91. http://dx.doi.org/10.1044/jslhr.4004.778.
Pełny tekst źródłaPak, Lale A., Kirill V. Savostyanov, Lyudmila M. Kuzenkova, Alexander A. Pushkov, Ilya S. Zhanin i Eugeniya V. Uvakina. "Molecular genetic diagnosis of speech disorders in children". L.O. Badalyan Neurological Journal 3, nr 1 (30.03.2022): 7–13. http://dx.doi.org/10.46563/2686-8997-2022-3-1-7-13.
Pełny tekst źródłaLuhrs, Kyleen, Tracey Ward, Caitlin M. Hudac, Jennifer Gerdts, Holly A. F. Stessman, Evan E. Eichler i Raphael A. Bernier. "Associations between Familial Rates of Psychiatric Disorders and De Novo Genetic Mutations in Autism". Autism Research and Treatment 2017 (2017): 1–9. http://dx.doi.org/10.1155/2017/9371964.
Pełny tekst źródłaCerniglia, Luca. "Neurobiological, Genetic, and Epigenetic Foundations of Eating Disorders in Youth". Children 11, nr 3 (23.02.2024): 274. http://dx.doi.org/10.3390/children11030274.
Pełny tekst źródłaGlotov, O. S., A. N. Chernov, P. A. Suchko, Yu A. Eismont i L. A. Mayorova. "Formation of cognitive processes in children with autism. Part II. Genetic mechanisms". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 69, nr 2 (8.05.2024): 26–33. http://dx.doi.org/10.21508/1027-4065-2024-69-2-26-33.
Pełny tekst źródłaKuraeva, Tamara Leonidovna, Elena Aleksandrovna Sechko, Lubov' Iosifovna Zilberman, Olga Nikolaevna Ivanova, Aleksandr Yurievich Mayorov, Ekaterina Olegovna Koksharova, Valentina Aleksandrovna Peterkova i Ivan Ivanovich Dedov. "Molecular genetic and clinical variants MODY2 and MODY3 in children in Russia". Problems of Endocrinology 61, nr 5 (28.01.2016): 14–25. http://dx.doi.org/10.14341/probl201561514-25.
Pełny tekst źródłaBelousova, E. D., O. S. Groznova i V. Yu Voinova. "Genome-wide sequencing in children with epilepsy and developmental disorders". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 69, nr 2 (10.05.2024): 56–64. http://dx.doi.org/10.21508/1027-4065-2024-69-2-56-64.
Pełny tekst źródłaCop, Esra, Pinar Yurtbasi, Ozgur Oner i Kerim Munir. "Genetic testing in children with autism spectrum disorders". Anatolian Journal of Psychiatry 16, nr 6 (2015): 426. http://dx.doi.org/10.5455/apd.1414607917.
Pełny tekst źródłaMokhtar, M. M. "Chromosomal aberrations in children with suspected genetic disorders". Eastern Mediterranean Health Journal 3, nr 1 (15.01.1997): 114–22. http://dx.doi.org/10.26719/1997.3.1.114.
Pełny tekst źródłaClarke, David. "Handbook of Neurodevelopmental and Genetic Disorders in Children". Journal of Applied Research in Intellectual Disabilities 14, nr 4 (grudzień 2001): 420–21. http://dx.doi.org/10.1111/j.1468-3148.2001.00080.x.
Pełny tekst źródłaGoldson, Edward. "Handbook of Neurodevelopmental and Genetic Disorders in Children",. Journal of Developmental & Behavioral Pediatrics 21, nr 4 (sierpień 2000): 307–8. http://dx.doi.org/10.1097/00004703-200008000-00013.
Pełny tekst źródłaTully, Elizabeth M. "Handbook of Neurodevelopmental and Genetic Disorders in Children". Journal of the American Academy of Child & Adolescent Psychiatry 39, nr 7 (lipiec 2000): 935. http://dx.doi.org/10.1097/00004583-200007000-00026.
Pełny tekst źródłaDONNELLY, CRAIG L. "Handbook of Neurodevelopmental and Genetic Disorders in Children". American Journal of Psychiatry 159, nr 6 (czerwiec 2002): 1070–71. http://dx.doi.org/10.1176/appi.ajp.159.6.1070.
Pełny tekst źródłaRapin, Isabelle. "Handbook of neurodevelopmental and genetic disorders in children". Annals of Neurology 47, nr 3 (marzec 2000): 415. http://dx.doi.org/10.1002/1531-8249(200003)47:3<415::aid-ana29>3.0.co;2-b.
Pełny tekst źródłaMaritska, Ziske, Atikah M. Ihsan, Ina Rahmawati, Perawati Perawati, Mohammad Hilal Atthariq Ramadhan, Bintang Arroyantri Prananjaya i Nita Parisa. "Genetic Conditions Associated with Intellectual Disability in Indonesian Population: A Review". Sriwijaya Journal of Medicine 7, nr 1 (10.06.2024): 8–15. http://dx.doi.org/10.32539/sjm.v7i1.220.
Pełny tekst źródłaChen, Lei-Shih, Jungkyung Min, Shixi Zhao, Yu-Chen Yeh i Tse-Yang Huang. "Information needs in genetic testing: A needs assessment survey among Taiwanese parents of children with autism spectrum disorders". Autism 23, nr 4 (3.08.2018): 902–9. http://dx.doi.org/10.1177/1362361318778903.
Pełny tekst źródłaGavryutina, Irina, Lawrence Fordjour i Vivian L. Chin. "Genetics of Thyroid Disorders". Endocrines 3, nr 2 (13.04.2022): 198–213. http://dx.doi.org/10.3390/endocrines3020018.
Pełny tekst źródłaWaters, A. M., B. P. Bradley i K. Mogg. "Biased attention to threat in paediatric anxiety disorders (generalized anxiety disorder, social phobia, specific phobia, separation anxiety disorder) as a function of ‘distress’versus‘fear’ diagnostic categorization". Psychological Medicine 44, nr 3 (17.04.2013): 607–16. http://dx.doi.org/10.1017/s0033291713000779.
Pełny tekst źródłaGorchkhanova, Z. K., E. A. Nikolaeva, S. V. Bochenkov i E. D. Belousova. "Clinical manifestations of Angelman syndrome in children". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 66, nr 6 (19.01.2022): 63–70. http://dx.doi.org/10.21508/1027-4065-2021-66-6-63-70.
Pełny tekst źródłaLelii, Mara, Elena Baggi, Laura Senatore, Maria Francesca Bedeschi, Robertino Dilena, Maria Iascone, Silvana Gangi, Paola Marchisio i Maria Francesca Patria. "Familial Sleep Disorders in Unknown Genetic Syndrome". Journal of Pediatric Genetics 09, nr 02 (21.10.2019): 132–36. http://dx.doi.org/10.1055/s-0039-1698808.
Pełny tekst źródłaLense, Miriam D., Eniko Ladányi, Tal-Chen Rabinowitch, Laurel Trainor i Reyna Gordon. "Rhythm and timing as vulnerabilities in neurodevelopmental disorders". Philosophical Transactions of the Royal Society B: Biological Sciences 376, nr 1835 (23.08.2021): 20200327. http://dx.doi.org/10.1098/rstb.2020.0327.
Pełny tekst źródłaGuzeva, Valentina I., Yulia A. Eremkina, Oksana V. Guzeva, Viktoriya V. Guzeva, Damir A. Malekov i Viktoriya A. Vedernikova. "Speech disorders in genetically determined forms of epilepsy in children. Clinical observations". Russian Military Medical Academy Reports 42, nr 4 (9.12.2023): 437–44. http://dx.doi.org/10.17816/rmmar585236.
Pełny tekst źródłaSorasio, Lorena, Luisa Franceschi, Lisa Pavinato i Antonella Peduto. "Quando il disturbo del neurosviluppo ha un substrato genetico: un caso di sindrome di Kleefstra". Medico e Bambino pagine elettroniche 24, nr 4 (30.04.2021): 114–17. http://dx.doi.org/10.53126/mebxxiv114.
Pełny tekst źródłaBOLTON, DEREK, THALIA C. ELEY, THOMAS G. O'CONNOR, SEAN PERRIN, SOPHIA RABE-HESKETH, FRÜHLING RIJSDIJK i PATRICK SMITH. "Prevalence and genetic and environmental influences on anxiety disorders in 6-year-old twins". Psychological Medicine 36, nr 3 (17.11.2005): 335–44. http://dx.doi.org/10.1017/s0033291705006537.
Pełny tekst źródłaBiesecker, Leslie G. "Clinical Commentary: The Law of Unintended Ethics". Journal of Law, Medicine & Ethics 25, nr 1 (1997): 16–18. http://dx.doi.org/10.1111/j.1748-720x.1997.tb01390.x.
Pełny tekst źródłaBanu, Meraj, Akbar Ali Khan Pathan i K. V. Chaitanya. "Diagnostics for Genetically Inherited Disorders: From Cytogenetics to Genomics Technologies- A Review". Biomedical and Pharmacology Journal 16, nr 2 (30.06.2023): 639–51. http://dx.doi.org/10.13005/bpj/2646.
Pełny tekst źródłaFolstein, Susan E., i Joseph Piven. "Etiology of Autism: Genetic Influences". Pediatrics 87, nr 5 (1.05.1991): 767–73. http://dx.doi.org/10.1542/peds.87.5.767.
Pełny tekst źródłaVolgina, S. Ya, A. R. Ahmetova, L. K. Shaidukova, N. V. Zhurkova i G. A. Kulakova. "The role of risk factors in the development of speech and language disorders in preschool children". Kazan medical journal 102, nr 4 (8.08.2021): 537–44. http://dx.doi.org/10.17816/kmj2021-537.
Pełny tekst źródłaErbeli, Florina, Marianne Rice i Silvia Paracchini. "Insights into Dyslexia Genetics Research from the Last Two Decades". Brain Sciences 12, nr 1 (26.12.2021): 27. http://dx.doi.org/10.3390/brainsci12010027.
Pełny tekst źródłaKalibataitė, Irma, Vilius Rutkauskas, Eglė Preikšaitienė i Vaidutis Kučinskas. "Establishing genetic diagnosis of intellectual disability in children: diagnostic yield of various genetic approaches". Acta medica Lituanica 19, nr 4 (31.01.2013): 409–15. http://dx.doi.org/10.6001/actamedica.v19i4.2550.
Pełny tekst źródłaGlotov, O. S., A. N. Chernov, P. A. Suchko, Yu A. Eismont i L. A. Mayorova. "Formation of cognitive processes in children with autism. Part I. Epigenetic mechanisms". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 69, nr 1 (7.03.2024): 34–44. http://dx.doi.org/10.21508/1027-4065-2024-69-1-34-44.
Pełny tekst źródłaSnetkov, A. I. "Diagnosis of genetic forms of rickets in children". N.N. Priorov Journal of Traumatology and Orthopedics 1, nr 3 (15.09.1994): 30–33. http://dx.doi.org/10.17816/vto105072.
Pełny tekst źródłaMountford, Hayley S., i Dianne F. Newbury. "The genomic landscape of language: Insights into evolution". Journal of Language Evolution 3, nr 1 (8.12.2017): 49–58. http://dx.doi.org/10.1093/jole/lzx019.
Pełny tekst źródłaNeumann, Alexander, Ilja M. Nolte, Irene Pappa, Tarunveer S. Ahluwalia, Erik Pettersson, Alina Rodriguez, Andrew Whitehouse i in. "A genome-wide association study of total child psychiatric problems scores". PLOS ONE 17, nr 8 (22.08.2022): e0273116. http://dx.doi.org/10.1371/journal.pone.0273116.
Pełny tekst źródłaRogers, Maureen. "Nail manifestations of some important genetic disorders in children". Dermatologic Therapy 15, nr 2 (czerwiec 2002): 111–20. http://dx.doi.org/10.1046/j.1529-8019.2002.01515.x.
Pełny tekst źródłaKarmiloff-Smith, A., D. D'Souza, T. M. Dekker, J. Van Herwegen, F. Xu, M. Rodic i D. Ansari. "Genetic and environmental vulnerabilities in children with neurodevelopmental disorders". Proceedings of the National Academy of Sciences 109, Supplement_2 (8.10.2012): 17261–65. http://dx.doi.org/10.1073/pnas.1121087109.
Pełny tekst źródłaAndersson, Nadine G., Maria Rossing, Marcus Fager Ferrari, Migle Gabrielaite, Eva Leinøe, Rolf Ljung, Annika Mårtensson, Eva Norström i Eva Zetterberg. "Genetic screening of children with suspected inherited bleeding disorders". Haemophilia 26, nr 2 (marzec 2020): 314–24. http://dx.doi.org/10.1111/hae.13948.
Pełny tekst źródłaHildebrand, Michael S., Victoria E. Jackson, Thomas S. Scerri, Olivia Van Reyk, Matthew Coleman, Ruth O. Braden, Samantha Turner i in. "Severe childhood speech disorder". Neurology 94, nr 20 (28.04.2020): e2148-e2167. http://dx.doi.org/10.1212/wnl.0000000000009441.
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