These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
202 related articles for article (PubMed ID: 23611254)
21. Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephaly. Kousar R; Nawaz H; Khurshid M; Ali G; Khan SU; Mir H; Ayub M; Wali A; Ali N; Jelani M; Basit S; Ahmad W; Ansar M J Child Neurol; 2010 Jun; 25(6):715-20. PubMed ID: 19808985 [TBL] [Abstract][Full Text] [Related]
22. Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein-truncating mutations of ASPM. Hussain S; Nawaz A; Hamid M; Ullah W; Khan IN; Afshan M; Rehman A; Nawaz H; Halswick J; Rehman SU; Ahmad S; Muzammal M; Muhammad N; Jan A; Khan S; Windpassinger C; Khan MA Biotechnol Appl Biochem; 2022 Dec; 69(6):2296-2303. PubMed ID: 34826358 [TBL] [Abstract][Full Text] [Related]
23. Genetic heterogeneity in Pakistani microcephaly families revisited. Ahmad I; Baig SM; Abdulkareem AR; Hussain MS; Sur I; Toliat MR; Nürnberg G; Dalibor N; Moawia A; Waseem SS; Asif M; Nagra H; Sher M; Khan MMA; Hassan I; Rehman SU; Thiele H; Altmüller J; Noegel AA; Nürnberg P Clin Genet; 2017 Jul; 92(1):62-68. PubMed ID: 28004384 [TBL] [Abstract][Full Text] [Related]
24. A Novel Frameshift Mutation in Abnormal Spindle-Like Microcephaly (ASPM) Gene in an Iranian Patient with Primary Microcephaly: A Case Report. Bazgir A; Agha Gholizadeh M; Sarvar F; Pakzad Z Iran J Public Health; 2019 Nov; 48(11):2074-2078. PubMed ID: 31970108 [TBL] [Abstract][Full Text] [Related]
25. A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family. Naqvi SF; Shabbir RMK; Tolun A; Basit S; Malik S Genet Test Mol Biomarkers; 2022 Jan; 26(1):37-42. PubMed ID: 35089071 [No Abstract] [Full Text] [Related]
26. Molecular analysis of 23 Pakistani families with autosomal recessive primary microcephaly using targeted next-generation sequencing. Wang R; Khan A; Han S; Zhang X J Hum Genet; 2017 Feb; 62(2):299-304. PubMed ID: 27784895 [TBL] [Abstract][Full Text] [Related]
27. Whole Exome Sequencing Identifies Three Novel Mutations in the Naseer MI; Abdulkareem AA; Muthaffar OY; Sogaty S; Alkhatabi H; Almaghrabi S; Chaudhary AG Front Pediatr; 2020; 8():627122. PubMed ID: 33643967 [TBL] [Abstract][Full Text] [Related]
28. Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM gene. Gul A; Hassan MJ; Mahmood S; Chen W; Rahmani S; Naseer MI; Dellefave L; Muhammad N; Rafiq MA; Ansar M; Chishti MS; Ali G; Siddique T; Ahmad W Neurogenetics; 2006 May; 7(2):105-10. PubMed ID: 16673149 [TBL] [Abstract][Full Text] [Related]
29. Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. Passemard S; Titomanlio L; Elmaleh M; Afenjar A; Alessandri JL; Andria G; de Villemeur TB; Boespflug-Tanguy O; Burglen L; Del Giudice E; Guimiot F; Hyon C; Isidor B; Mégarbané A; Moog U; Odent S; Hernandez K; Pouvreau N; Scala I; Schaer M; Gressens P; Gerard B; Verloes A Neurology; 2009 Sep; 73(12):962-9. PubMed ID: 19770472 [TBL] [Abstract][Full Text] [Related]
30. [Genetic analysis of a child with autosomal recessive primary microcephaly due to variant of ASPM gene and a literature review]. Wang J; Wang X; Zhang L; Huang Y; Sha R; An J; Wu Y; Guo Z; Jia Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Oct; 41(10):1243-1248. PubMed ID: 39344621 [TBL] [Abstract][Full Text] [Related]
32. 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; 47(12):823-8. PubMed ID: 20978018 [TBL] [Abstract][Full Text] [Related]
33. Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally. Desir J; Cassart M; David P; Van Bogaert P; Abramowicz M Am J Med Genet A; 2008 Jun; 146A(11):1439-43. PubMed ID: 18452193 [TBL] [Abstract][Full Text] [Related]
34. Novel and recurrent ASPM mutations of founder effect in Chinese population. Li M; Luo J; Yang Q; Chen F; Chen J; Qin J; He W; Chen J; Yi S; Qin Z; Yi S; Huang L; Qiu X; Pan P; Luo J; Shen Y Brain Dev; 2022 Sep; 44(8):540-545. PubMed ID: 35491272 [TBL] [Abstract][Full Text] [Related]
35. A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene. Ghafouri-Fard S; Fardaei M; Gholami M; Miryounesi M Gene; 2015 Oct; 571(1):149-50. PubMed ID: 26192461 [TBL] [Abstract][Full Text] [Related]
36. A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly. Akbariazar E; Ebrahimpour M; Akbari S; Arzhanghi S; Abedini SS; Najmabadi H; Kahrizi K Iran J Child Neurol; 2013; 7(2):23-30. PubMed ID: 24665293 [TBL] [Abstract][Full Text] [Related]
37. Modifier Genes in Microcephaly: A Report on Makhdoom EUH; Waseem SS; Iqbal M; Abdullah U; Hussain G; Asif M; Budde B; Höhne W; Tinschert S; Saadi SM; Yousaf H; Ali Z; Fatima A; Kaygusuz E; Khan A; Jameel M; Khan S; Tariq M; Anjum I; Altmüller J; Thiele H; Höning S; Baig SM; Nürnberg P; Hussain MS Genes (Basel); 2021 May; 12(5):. PubMed ID: 34068194 [TBL] [Abstract][Full Text] [Related]