Որոնման արդյունքները - "dwarfism"

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

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Clinical manifestations of Ellis-van Creveld syndrome ‌ 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 ‌ 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 ‌ 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 ‌ 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 ‌ Kseniya O. Samsonova

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Seckel syndrome: A rare case report ‌ 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 ‌ Sameeulla Shaik, Jayam Raviraj, Suresh Dirasantchu, Suman S Venkata

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

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

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Becker's nevus syndrome ‌ 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 ‌ Li Zhang, Jingfei Liu, Dianyong Gao, Dong Li

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KIDNEY INVOLVEMENT IN SECKEL SYNDROME ‌ 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 ‌ 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 ‌ 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 ‌ 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 ‌ 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 ‌ 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 ‌ 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 ‌ Q.C. Wu, W.B. Wang, L. Sun, Y.S. Xu, X.J. Xie, X.M. Ma, Z.Y. Su

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