المؤلفون: Ivan Y. Iourov, Svetlana G. Vorsanova, Yuri B. Yurov, Thomas Bertrand

المصدر: Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-6 (2018)

مصطلحات موضوعية: Chromosome X, Rare disorders, Rare chromosome disorders, Rett syndrome, Translational medical research, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13039-018-0412-2; https://doaj.org/toc/1755-8166

URL الوصول: https://doaj.org/article/b2b10a4c4dfc4496a0be5a54d95cdfd5

المؤلفون: Svetlana G. Vorsanova, Ivan Y. Iourov, Thomas Bertrand, Yuri B. Yurov

المصدر: Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-6 (2018)
Molecular Cytogenetics

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, History, Chromosome X, lcsh:QH426-470, Local Development, education, Context (language use), Rett syndrome, Review, Biochemistry, MECP2, 03 medical and health sciences, Rare chromosome disorders, Health care, Genetics, medicine, Psychiatry, Molecular Biology, Genetics (clinical), health care economics and organizations, business.industry, Biochemistry (medical), medicine.disease, humanities, lcsh:Genetics, 030104 developmental biology, Rare disorders, Molecular Medicine, Translational medical research, business, Rare disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e093ace6845d4d78868da2feca52d320
http://link.springer.com/article/10.1186/s13039-018-0412-2

المؤلفون: Linda Gilmore

المصدر: Cypriot Journal of Educational Sciences, Vol 09, Iss 01, Pp 14-20 (2014)

مصطلحات موضوعية: chromosome abnormalities, chromosomes, chromosome disorders, lcsh:L, rare chromosome disorders, lcsh:Education

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doajarticles::4452fab09d450e5f670d98d17edd67f1
http://www.world-education-center.org/index.php/cjes/article/view/2-2/pdf_248

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المصدر: Research and Practice in Intellectual and Developmental Disabilities

مصطلحات الفهرس: Family support, information, rare chromosome disorders, unique, Contribution to Journal

URL: https://eprints.qut.edu.au/223223/1/112689.pdf
https://eprints.qut.edu.au/223223/1/112689.pdf
doi:10.1080/23297018.2017.1360152
Gilmore, Linda (2018) Supporting families of children with rare and unique chromosome disorders. Research and Practice in Intellectual and Developmental Disabilities, 5(1), pp. 8-16.

المصدر: 16th SSBP International Research Symposium

مصطلحات الفهرس: 16p duplication, behavioural phenotype, rare chromosome disorders, Contribution to conference

URL: https://eprints.qut.edu.au/83627/7/83627_GILMORE_Variable%20Phenotype_CONF%20FINAL%20DRAFT.pdf
http://www.ssbpconference.org/docs/stellenbosch_conference_book_2013.pdf
https://eprints.qut.edu.au/83627/7/83627_GILMORE_Variable%20Phenotype_CONF%20FINAL%20DRAFT.pdf
http://www.ssbpconference.org/docs/stellenbosch_conference_book_2013.pdf
Gilmore, Linda, Good, Lisa, Leong, Eliza Weiqin, Heussler, Helen, & Bowling, Francis (2013) Variable phenotype in 16p duplication within a family. In 16th SSBP International Research Symposium, 2013-09-12 - 2013-09-14.

مصطلحات الفهرس: children, rare chromosome disorders, siblings, support, Other Contribution

URL: https://eprints.qut.edu.au/52927/22/52927.pdf
https://eprints.qut.edu.au/52927/23/2012004037.pdf
http://www.rarechromo.org/information/Other/Supporting%20Siblings%20of%20Children%20with%20a%20Rare%20Chromosome%20Disorder%20FTNW.pdf
https://eprints.qut.edu.au/52927/22/52927.pdf
https://eprints.qut.edu.au/52927/23/2012004037.pdf
http://www.rarechromo.org/information/Other/Supporting%20Siblings%20of%20Children%20with%20a%20Rare%20Chromosome%20Disorder%20FTNW.pdf
Gilmore, Linda, Waugh, Melanie, Haynes, Allison, Hearne, Carley, Mercer, Charlotte, & Wilson, Kimberley (2012) Supporting siblings of children with a rare chromosome disorder [Chromosome Disorder Leaflets]. Unique - The Rare Chromosome Disorder Support Group.