অনুসন্ধান ফলাফলগুলি - "Seckel syndrome"

Seckel Syndrome with Holoprosencephaly অনুযায়ী J Gordon Millichap

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

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

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Anesthetic management of a child with Seckel syndrome for multiple extractions and restoration of teeth অনুযায়ী Suman Arora, Babita Ghai, Vidya Rattan

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Virchow-Seckel Type Bird Headed Dwarfism (Seckel Syndrome) - A Case Report অনুযায়ী K N Sumanth, V C Vinod, Prerna Taneja

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Progenitor death drives retinal dysplasia and neuronal degeneration in a mouse model of ATRIP-Seckel syndrome অনুযায়ী Gabriel E. Matos-Rodrigues, Pedro B. Tan, Maurício Rocha-Martins, Clara F. Charlier, Anielle L. Gomes, Felipe Cabral-Miranda, Paulius Grigaravicius, Thomas G. Hofmann, Pierre-Olivier Frappart, Rodrigo A. P. Martins

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The Seckel syndrome: A case observed in the pediatric department of the University Hospital Center Sourou Sanou (Burkina Faso) অনুযায়ী Ad Bafa Ibrahim Ouattara, Makoura Barro, Sahoura Fatimata Nacro, Ibraïma Traoré, Bintou Sanogo, Jean W. Diallo, Boubacar Nacro

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Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders অনুযায়ী Andrey V. Marakhonov, Fedor A. Konovalov, Amin Kh. Makaov, Tatyana A. Vasilyeva, Vitaly V. Kadyshev, Varvara A. Galkina, Elena L. Dadali, Sergey I. Kutsev, Rena A. Zinchenko

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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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Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in <i>RTTN</i> Gene: A Seckel Syndrome Case Report অনুযায়ী Behjat Ul Mudassir, Zehra Agha

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

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First person - Gabriel Matos-Rodrigues

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Aicardi-Goutières syndrome with SAMHD1 deficiency can be diagnosed by unscheduled DNA synthesis test অনুযায়ী Chikako Senju, Chikako Senju, Chikako Senju, Chikako Senju, Chikako Senju, Yuka Nakazawa, Yuka Nakazawa, Yuka Nakazawa, Mayuko Shimada, Mayuko Shimada, Mayuko Shimada, Dai Iwata, Dai Iwata, Michiko Matsuse, Katsumi Tanaka, Yasushi Miyazaki, Shinichi Moriwaki, Norisato Mitsutake, Tomoo Ogi, Tomoo Ogi, Tomoo Ogi

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The rare DNA ligase IV syndrome: A case report অনুযায়ী Petroula Gerasimou, Laura Koumas, Andri Miltiadous, Ioannis Kyprianou, Jianxiang Chi, Rafaella Gavrielidou, Elena Socratous, Loizos Loizou, Eleni Papachristodoulou, Evagelia Karaoli, Anastasios Loizos, Violetta Anastasiadou, Paul Costeas

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