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Journal Abstract Search
130 related items for PubMed ID: 21957340
1. Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3). Vundinti BR, Kerketta L, Korgaonkar S, Ghosh K. Indian J Hum Genet; 2007 Jan; 13(1):33-5. PubMed ID: 21957340 [Abstract] [Full Text] [Related]
2. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion. Chen CP, Chang TY, Shih JC, Lin SP, Lin CJ, Wang W, Lee CC, Town DD, Pan CW, Tzen CY. Prenat Diagn; 2002 Dec; 22(12):1063-6. PubMed ID: 12454959 [Abstract] [Full Text] [Related]
3. Phenotypic and cytogenetic spectrum of 9p trisomy. Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM. Genet Couns; 2007 Dec; 18(1):29-48. PubMed ID: 17515299 [Abstract] [Full Text] [Related]
4. [Analysis of a pedigree with partial trisomy 9 and partial monosomy 13 derived from a maternal balanced t(9;13) translocation]. Sha Y, Mei L, Ji Z, Wang X, Lin S, Li L. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Apr 10; 36(4):336-339. PubMed ID: 30950020 [Abstract] [Full Text] [Related]
7. Maternal origin of a unique extra chromosome, der(9)(pter-->q13::q13-->q12:) in a girl with typical trisomy 9p syndrome. Teraoka M, Narahara K, Yokoyama Y, Ninomiya S, Mizuta S, Une T, Seino Y. Am J Med Genet; 2001 Jul 22; 102(1):25-8. PubMed ID: 11471168 [Abstract] [Full Text] [Related]
8. A Case of X-linked Intellectual Disability with Novel Chromosome 9p12-pter Unbalanced Translocation on Chromosome Xp. Maeda K, Sugihara Y. Intern Med; 2024 Sep 27. PubMed ID: 39343574 [Abstract] [Full Text] [Related]
9. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation. Brambila-Tapia AJ, Neira VA, Vásquez-Velásquez AI, Jimenez-Arredondo RE, Chávez-González EL, Picos-Cárdenas VJ, Fletes-Rayas AL, Figuera LE. Genet Couns; 2014 Sep 27; 25(3):289-97. PubMed ID: 25365851 [Abstract] [Full Text] [Related]
10. [A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)]. Woo KS, Kim KE, Kwon EY, Kim JP, Han JY. Korean J Lab Med; 2008 Apr 27; 28(2):155-9. PubMed ID: 18458513 [Abstract] [Full Text] [Related]
11. Absence of 9q22-9qter in trisomy 9 does not prevent a Dandy-Walker phenotype. von Kaisenberg CS, Caliebe A, Krams M, Hackelöer BJ, Jonat W. Am J Med Genet; 2000 Dec 18; 95(5):425-8. PubMed ID: 11146460 [Abstract] [Full Text] [Related]
12. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter). Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W. Genet Couns; 2006 Dec 18; 17(1):57-63. PubMed ID: 16719278 [Abstract] [Full Text] [Related]
13. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation]. Wang XR, Luo RL, Dai XH, Liu JY. Yi Chuan; 2007 Jul 18; 29(7):813-6. PubMed ID: 17646146 [Abstract] [Full Text] [Related]
14. Dandy-Walker malformation in an infant with tetrasomy 9p. Cazorla Calleja MR, Verdú A, Félix V. Brain Dev; 2003 Apr 18; 25(3):220-3. PubMed ID: 12689705 [Abstract] [Full Text] [Related]
15. Array-CGH study of partial trisomy 9p without mental retardation. Bouhjar IB, Hannachi H, Zerelli SM, Labalme A, Gmidène A, Soyah N, Missaoui S, Sanlaville D, Elghezal H, Saad A. Am J Med Genet A; 2011 Jul 18; 155A(7):1735-9. PubMed ID: 21626676 [Abstract] [Full Text] [Related]
16. Prenatal diagnosis of tetrasomy 9p with Dandy-Walker malformation. Hengstschläger M, Bettelheim D, Drahonsky R, Repa C, Deutinger J, Bernaschek G. Prenat Diagn; 2004 Aug 18; 24(8):623-6. PubMed ID: 15305350 [Abstract] [Full Text] [Related]
17. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p). Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Genet Couns; 1998 Aug 18; 9(3):215-21. PubMed ID: 9777345 [Abstract] [Full Text] [Related]
18. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature. Mishra R, Paththinige CS, Sirisena ND, Nanayakkara S, Kariyawasam UGIU, Dissanayake VHW. BMC Pediatr; 2018 Jan 08; 18(1):4. PubMed ID: 29310616 [Abstract] [Full Text] [Related]
19. Duplication 9p and their implication to phenotype. Guilherme RS, Meloni VA, Perez AB, Pilla AL, de Ramos MA, Dantas AG, Takeno SS, Kulikowski LD, Melaragno MI. BMC Med Genet; 2014 Dec 20; 15():142. PubMed ID: 25526829 [Abstract] [Full Text] [Related]
20. [Systematic genetic analysis for a case with duplication 9p]. Zhang J, Li H, Jiang S, Li H, Zhang Y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr 20; 32(2):237-9. PubMed ID: 25863095 [Abstract] [Full Text] [Related] Page: [Next] [New Search]