অনুসন্ধান ফলাফলগুলি - "dwarfism"

Bird-Headed Dwarf of Seckel অনুযায়ী Harsha Vardhan B, Muthu M, Saraswathi K, Koteeswaran D

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Clinical manifestations of Ellis-van Creveld syndrome অনুযায়ী Vinay C, Reddy R, Uloopi K, Sekhar R

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A case of thanatophoric dysplasia type I with an R248C mutation in the gene অনুযায়ী Eun Jung Noe, Han Wook Yoo, Kwang Nam Kim, So Yeon Lee

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Thanatophoric dysplasia: case report of an autopsy complemented by postmortem computed tomographic study অনুযায়ী Éber Emanuel Mayoral, Regina Schultz, Sérgio Rosemberg, Lisa Suzuki, Luiz Antonio Nunes de Oliveira, Fernando Uliana Kay

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Seckel syndrome: A report of a case অনুযায়ী K Ramalingam, S D Kaliyamurthy, M Govindarajan, S Swathi

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Beauty and ugliness as endocrine pathology: a look through the prism of history and art অনুযায়ী Kseniya O. Samsonova

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Seckel syndrome: A rare case report অনুযায়ী Rinky Sisodia, Ravi Kadur Sundar Raj, Vipin Goel

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Ellis-van Creveld syndrome with unusual oral and dental findings: A rare clinical entity অনুযায়ী Sameeulla Shaik, Jayam Raviraj, Suresh Dirasantchu, Suman S Venkata

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Hypertrophic cardiomyopathy with Jeune syndrome: The first reported case অনুযায়ী Osman Güvenç, Saime Sündüs Uygun, Derya Çimen, Eyüp Aslan, Ali Annagür

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Orofacial manifestations of congenital hypothyroidism: Clinicoradiological case report অনুযায়ী Gundareddy N Suma, Manisha Lakhanpal, Manu Dhillon, Siddharth Srivastava

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Becker's nevus syndrome অনুযায়ী Sathyanarayana B Dasegowda, GB Basavaraj, KC Nischal, MR Swaroop, NP Umashankar, Suchetha S Swamy

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Role of ghrelin in promoting catch-up growth and maintaining metabolic homeostasis in small-for-gestational-age infants অনুযায়ী Li Zhang, Jingfei Liu, Dianyong Gao, Dong Li

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KIDNEY INVOLVEMENT IN SECKEL SYNDROME অনুযায়ী Tudor Lazaruc, Iuliana Magdalena Starcea, Anca Ivanov, Georgiana Scurtu, Maria Adriana Mocanu, Vasile Valeriu Lupu, Ancuta Lupu, Roxana Alexandra Bogos, Ingrith Miron, Lavinia Bodescu Amancei - Ionescu

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PRACTICAL ASPECTS INVOLVED IN TECHNOLOGICAL ALGORITHM FOR MAKING FIXED PROTHESES USING DIGITAL METHODS অনুযায়ী Irina Grădinaru, Alice Arina Ciocan Pendefunda, Loredana Liliana Hurjui, Balcoș Carina, Mihaela Mitrea, Oana Adina Armencia, Magda Ecaterina Antohe

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Central precocious puberty with hypothalamic hamartoma: the first case reports of 2 siblings with different phenotypes of Seckel syndrome 5 অনুযায়ী Jisun Park, Minjun Jeon, Seri Maeng, Dae Kyu Kwon, Sujin Kim, Ji Eun Lee

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Oral manifestations in child patient with Ellis-van Creveld syndrome: case report অনুযায়ী Lucas Fernando Oliveira Tomáz Ferraresso, Fabio Anevan Ubiski Fagundes, Mariella Padovese, Paola Singi, Cássia Cilene Dezan Garbelini, Farli Aparecida Carrilho Boer

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First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene অনুযায়ী Alain Chebly, Sandra Corbani, Joelle Abou Ghoch, Cybel Mehawej, André Megarbane, Eliane Chouery

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Possibilities of using modern standards to assess the physical development of children with cerebral palsy অনুযায়ী I. A. Leontiev, E. P. Sitnikova, M. V. Kovina

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Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2 অনুযায়ী Erdal Eren, Havva Tezcan Ünlü, Serdar Ceylaner, Ömer Tarım

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Mutation analysis of the fibroblast growth factor receptor 3 gene in fetuses with thanatophoric dysplasia, type I অনুযায়ী Q.C. Wu, W.B. Wang, L. Sun, Y.S. Xu, X.J. Xie, X.M. Ma, Z.Y. Su

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