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197 related items for PubMed ID: 31624053
21. Many roads lead to primary autosomal recessive microcephaly. Kaindl AM, Passemard S, Kumar P, Kraemer N, Issa L, Zwirner A, Gerard B, Verloes A, Mani S, Gressens P. Prog Neurobiol; 2010 Mar; 90(3):363-83. PubMed ID: 19931588 [Abstract] [Full Text] [Related]
23. Identification of Pathogenic Mutations in Primary Microcephaly- (MCPH-) Related Three Genes CENPJ, CASK, and MCPH1 in Consanguineous Pakistani Families. Khan NM, Masoud MS, Baig SM, Qasim M, Chang J. Biomed Res Int; 2022 Mar; 2022():3769948. PubMed ID: 35281599 [Abstract] [Full Text] [Related]
25. Misregulated chromosome condensation in MCPH1 primary microcephaly is mediated by condensin II. Trimborn M, Schindler D, Neitzel H, Hirano T. Cell Cycle; 2006 Feb; 5(3):322-6. PubMed ID: 16434882 [Abstract] [Full Text] [Related]
26. Deficient adaptation to centrosome duplication defects in neural progenitors causes microcephaly and subcortical heterotopias. González-Martínez J, Cwetsch AW, Martínez-Alonso D, López-Sainz LR, Almagro J, Melati A, Gómez J, Pérez-Martínez M, Megías D, Boskovic J, Gilabert-Juan J, Graña-Castro O, Pierani A, Behrens A, Ortega S, Malumbres M. JCI Insight; 2021 Aug 23; 6(16):. PubMed ID: 34237032 [Abstract] [Full Text] [Related]
27. Genetic heterogeneity in Pakistani microcephaly families. Sajid Hussain M, Marriam Bakhtiar S, Farooq M, Anjum I, Janzen E, Reza Toliat M, Eiberg H, Kjaer KW, Tommerup N, Noegel AA, Nürnberg P, Baig SM, Hansen L. Clin Genet; 2013 May 23; 83(5):446-51. PubMed ID: 22775483 [Abstract] [Full Text] [Related]
32. CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects. Nasser H, Vera L, Elmaleh-Bergès M, Steindl K, Letard P, Teissier N, Ernault A, Guimiot F, Afenjar A, Moutard ML, Héron D, Alembik Y, Momtchilova M, Milani P, Kubis N, Pouvreau N, Zollino M, Guilmin Crepon S, Kaguelidou F, Gressens P, Verloes A, Rauch A, El Ghouzzi V, Drunat S, Passemard S. J Med Genet; 2020 Jun 23; 57(6):389-399. PubMed ID: 32015000 [Abstract] [Full Text] [Related]
35. A clinical and molecular genetic study of 112 Iranian families with primary microcephaly. Darvish H, Esmaeeli-Nieh S, Monajemi GB, Mohseni M, Ghasemi-Firouzabadi S, Abedini SS, Bahman I, Jamali P, Azimi S, Mojahedi F, Dehghan A, Shafeghati Y, Jankhah A, Falah M, Soltani Banavandi MJ, Ghani M, Garshasbi M, Rakhshani F, Naghavi A, Tzschach A, Neitzel H, Ropers HH, Kuss AW, Behjati F, Kahrizi K, Najmabadi H. J Med Genet; 2010 Dec 23; 47(12):823-8. PubMed ID: 20978018 [Abstract] [Full Text] [Related]
37. The Yin and Yang of Autosomal Recessive Primary Microcephaly Genes: Insights from Neurogenesis and Carcinogenesis. Zhou X, Zhi Y, Yu J, Xu D. Int J Mol Sci; 2020 Mar 01; 21(5):. PubMed ID: 32121580 [Abstract] [Full Text] [Related]