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  1. 861
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    Genetic analysis of a pedigree with MECP2 duplication syndrome in China by Lan Zeng, Hui Zhu, Jin Wang, Qiyan Wang, Ying Pang, Zemin Luo, Ai Chen, Shengfang Qin, Shuyao Zhu

    Published 2024
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  2. 862
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    Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family by Panlai Shi, Conghui Wang, Yuting Zheng, Xiangdong Kong

    Published 2021
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  3. 863
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    Adolescent gambling behavior: a gender oriented prevention strategy is required? by Alessandra Buja, Milena Sperotto, Bruno Genetti, Paolo Vian, Fabio Vittadello, Elisabetta Simeoni, Chiara Zampieri, Vincenzo Baldo

    Published 2022
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  4. 864
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    Blau syndrome with a rare mutation in exon 9 of NOD2 gene by Jelena Velickovic, Fatma Silan, Firdevs Dincsoy Bir, Coskun Silan, Burcu Albuz, Ozturk Ozdemir

    Published 2019
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  5. 865
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    XERODERMA PIGMENTOSO DE KAPOSI: PRESENTACION DE UN CASO Xeroderma Pigmentosum: A case presentation by Heizel Escobar Vega, Alexey Expósito Jalturin, Eloida López Hernández

    Published 2009
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  6. 866
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    PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China by Jing WANG, Yuanzhi XU, Jing CHEN, Feiyu WANG, Renhuan HUANG, Songtao WU, Linjing SHU, Jingyi QIU, Zhi YANG, Junjie XUE, Raorao WANG, Jilin ZHAO, Wenli LAI

    Published 2013
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  7. 867
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    Epidemiologic study of familial Type 2 diabetes in Tehran by Mostafa Najafipour, Masoumeh Zareizadeh, Farzad Najafipour

    Published 2018
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  8. 868
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    Souvenirs Related to Ignacy Łukasiewicz in the Collection of the Pharmacy Museum at Jagiellonian University Medical College by Iwona Ewa Dymarczyk

    Published 2022
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  9. 869
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    Avoiding the Subject Media, Culture and the Object by Clemens, Justin

    Published 2004
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  10. 870
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    Management of Educational Administration of Semarang Police Academy by Salafudin , Moh. Anwar

    Published 2012
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  11. 871
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    Kebahagiaan Pada Lanjut Usia Ditinjau Dari Dukungan Keluarga by Ayu Mastuti, Dyah, , Santi Sulandari, S.Psi, .M. Ger

    Published 2016
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  12. 872
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    Cara Mengatasi Masalah Pada Siswa SMP Yang Terindikasi Conduct Problem by Novita Luthfiana, Dhini, , Usmi Karyani S.Psi, M.Si., Psi

    Published 2017
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  13. 873
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    The Major Discoveries of Cajal and His Disciples: Consolidated Milestones for the Neuroscience of the XXIst Century by Miguel A. Merchan

    Published 2017
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  14. 874
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    Contro frate Bernardino da Siena. Processi al maestro Amedeo Landi (Milano 1437-1447)

    Published 2021
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  15. 875
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    El estrés y el niño. Factores de estrés durante la infancia by María Teresa GONZÁLEZ MARTÍNEZ, María Luz GARCÍA GONZÁLEZ

    Published 2009
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  16. 876
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    Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation by Xue Gong, Yunru He, Guoyan Lu, Yulin Zhang, Yu Qiu, Lina Qiao, Yifei Li

    Published 2022
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  17. 877
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    A novel start-loss mutation of the SLC29A3 gene in a consanguineous family with H syndrome: clinical characteristics, in silico analysis and literature review by Nahid Rezaie, Nader Mansour Samaei, Ayda Ghorbani, Naghmeh Gholipour, Shohreh Vosough, Mahboobeh Rafigh, Abolfazl Amini

    Published 2024
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  18. 878
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    Three Cases of Bilateral Breast Absence Associated with Familial Congenital Ectodermal Defects by Su S, Xie R, Ding X, Lin Y

    Published 2021
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  19. 879
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    METAFUNCTION PATTERNS OF THE TOBA BATAK LANGUAGE by Hepnyi Samosir

    Published 2018
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  20. 880
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    Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports by Katja Kloth, Matthis Synofzik, Christoph Kernstock, Simone Schimpf-Linzenbold, Frank Schuettauf, Axel Neu, Bernd Wissinger, Nicole Weisschuh

    Published 2019
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