المؤلفون: Hend T. El-Borm, Marwa S. Gobara, Gamal M. Badawy

المصدر: Beni-Suef University Journal of Basic and Applied Sciences, Vol 12, Iss 1, Pp 1-12 (2023)

مصطلحات موضوعية: Labetalol, Ginger, Skeletal malformation, Fetal liver, Cell cycle, Apoptosis, Medicine (General), R5-920, Science

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2314-8543Test

الوصول الحر: https://doaj.org/article/d7ac9707352e4070917a3c32598595ccTest

المؤلفون: Almeida, Gustavo Luiz Gouvêa de, Almeida, Marcelo Barbosa de, Santos, Ana Carolina Mendes dos, Vargas, Ângela, Ballot, Sophie, Santos, Liana Monteiro

المصدر: Research, Society and Development; Vol. 12 No. 14; e20121444487 ; Research, Society and Development; Vol. 12 Núm. 14; e20121444487 ; Research, Society and Development; v. 12 n. 14; e20121444487 ; 2525-3409

مصطلحات موضوعية: Diaphragmatic hernia, Skeletal malformation, Cat., Anomalia esquelética, Hérnia diafragmática, Gato, Hernia diafragmática, Malformaciones esqueléticas

وصف الملف: application/pdf

العلاقة: https://rsdjournal.org/index.php/rsd/article/view/44487/35579Test; https://rsdjournal.org/index.php/rsd/article/view/44487Test

الإتاحة: https://doi.org/10.33448/rsd-v12i14.44487Test
https://rsdjournal.org/index.php/rsd/article/view/44487Test

المؤلفون: Manoj Arya, Rajendra Shakunt, Anoop Raj Singh, Shipra Verma, Vinay Kanaujia

المصدر: Journal of Clinical and Diagnostic Research, Vol 16, Iss 11, Pp RD01-RD03 (2022)

مصطلحات موضوعية: congenital disorder, hallux valgus, heterotrophic ossification, skeletal malformation, Medicine

وصف الملف: electronic resource

العلاقة: https://jcdr.net/articles/PDF/16978/58313_CETest(arnp)_F[SK]_PF1(SC_KM)_PFA(SC_KM)_PF2(AvG_KM)_PN(KM).pdf; https://doaj.org/toc/2249-782XTest; https://doaj.org/toc/0973-709XTest

الوصول الحر: https://doaj.org/article/b6b1c2222c8a435caa362ca536a0c395Test

المؤلفون: Chuan Zhang, Shengju Hao, ZhaoYan Meng, Ling Hui, Yan Wang, Feng Xuan, Xue Chen, Xing Wang, Furong Zheng, Lei Zheng, Bingbo Zhou, Xinqi Wu, Qinghua Zhang, Zongfu Cao

المصدر: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-6 (2021)

مصطلحات موضوعية: MPS II, IDS, Developmental delay, Special face, Skeletal malformation, Internal medicine, RC31-1245, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1755-8794Test

الوصول الحر: https://doaj.org/article/713aa05d65d2495096c771d6956cd637Test

المؤلفون: Chopra, Sameer S., Leshchiner, Ignaty, Duzkale, Hatice, McLaughlin, Heather, Giovanni, Monica, Zhang, Chengsheng, Stitziel, Nathan, Fingeroth, Joyce D., Joyce, Robin M., Lebo, Matthew, Rehm, Heidi, Vuzman, Dana, Maas, Richard, Sunyaev, Shamil R., Murray, Michael, Cassa, Christopher A.

المساهمون: Department of Medicine, Division of Infectious Diseases and Immunology

المصدر: Molecular genetics and genomic medicine ; 3 ; 5 ; 413-23

مصطلحات موضوعية: CHST11, inherited lymphoproliferative disorder, malignant lymphoproliferative disorder, MIR3922, skeletal malformation, Genomics, Hemic and Lymphatic Diseases, Molecular Genetics, Musculoskeletal Diseases

العلاقة: Link to Article in PubMed; Mol Genet Genomic Med. 2015 Sep;3(5):413-23. doi:10.1002/mgg3.152. Epub 2015 May 10. Link to article on publisher's site; 2324-9269 (Linking); http://hdl.handle.net/20.500.14038/39821Test; https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3623&context=oapubs&unstamped=1Test; https://escholarship.umassmed.edu/oapubs/2619Test; 7920037; oapubs/2619

الإتاحة: https://doi.org/10.1002/mgg3.152Test
https://doi.org/20.500.14038/39821Test
https://hdl.handle.net/20.500.14038/39821Test
https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3623&context=oapubs&unstamped=1Test
https://escholarship.umassmed.edu/oapubs/2619Test

المؤلفون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A.

المساهمون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A., Yeditepe Üniversitesi

مصطلحات موضوعية: CHST11, Inherited lymphoproliferative disorder, Malignant lymphoproliferative disorder, MIR3922, Skeletal malformation

العلاقة: Molecular Genetics and Genomic Medicine; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 413; 423; https://hdl.handle.net/20.500.11831/1568Test

الإتاحة: https://doi.org/20.500.11831/1568Test
https://hdl.handle.net/20.500.11831/1568Test

المؤلفون: Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA

المساهمون: Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA, Yeditepe Üniversitesi

مصطلحات موضوعية: CHST11, inherited lymphoproliferative disorder, malignant lymphoproliferative disorder, MIR3922, skeletal malformation

العلاقة: MOLECULAR GENETICS & GENOMIC MEDICINE; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; WOS: 000214715600006; PubMed ID: 26436107; 413; 423; https://hdl.handle.net/20.500.11831/1571Test

الإتاحة: https://doi.org/20.500.11831/1571Test
https://hdl.handle.net/20.500.11831/1571Test

المؤلفون: Hiroshi Kitoh

المصدر: Biomedicines; Volume 8; Issue 9; Pages: 325

مصطلحات موضوعية: fibrodysplasia ossificans progressiva, skeletal malformation, heterotopic ossification, clinical trials

وصف الملف: application/pdf

العلاقة: Cell Biology and Pathology; https://dx.doi.org/10.3390/biomedicines8090325Test

الإتاحة: https://doi.org/10.3390/biomedicines8090325Test

المؤلفون: Dongdong Wang, Mengmeng Zhang, Haixia Guan, Xiaoli Wang

المصدر: Frontiers in Endocrinology, Vol 10 (2019)

مصطلحات موضوعية: pituitary stalk interruption syndrome, osteogenesis imperfecta, case report, next generation sequencing, skeletal malformation, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/article/10.3389/fendo.2019.00193/fullTest; https://doaj.org/toc/1664-2392Test

الوصول الحر: https://doaj.org/article/e92c8bea27da4aac98c714b063edbe98Test

المؤلفون: Salvaggio, Antonio, MARINO, Fabio, Albano, Marco, Pecoraro, Roberta, Camiolo, Giuseppina, Tibullo, Daniele, Bramanti, Vincenzo, Lombardo, Bianca M., Saccone, Salvatore, Mazzei, Veronica, Brundo, Maria V.

المساهمون: Salvaggio, Antonio, Marino, Fabio, Albano, Marco, Pecoraro, Roberta, Camiolo, Giuseppina, Tibullo, Daniele, Bramanti, Vincenzo, Lombardo, Bianca M., Saccone, Salvatore, Mazzei, Veronica, Brundo, Maria V.

مصطلحات موضوعية: Bone development, Calcein, Skeletal malformation, Zebrafish, Zinc chloride, Physiology, Physiology (medical)

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27199768; info:eu-repo/semantics/altIdentifier/wos/WOS:000443547500001; volume:7; issue:APR; firstpage:1; lastpage:6; numberofpages:6; journal:FRONTIERS IN PHYSIOLOGY; http://hdl.handle.net/11570/3102066Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84966327433; https://www.frontiersin.org/articles/10.3389/fphys.2016.00153/fullTest

الإتاحة: https://doi.org/10.3389/fphys.2016.00153Test
http://hdl.handle.net/11570/3102066Test