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.
120 related articles for article (PubMed ID: 31922597)
21. [Balanced chromosomal rearrangements resulting in intellectual disability. An analysis of 22 cases with application of CGH and FISH methods]. Borg K; Bocian E; Bernaciak J; Nowakowska B; Derwińska K; Obersztyn E; Szczałuba K; Smigiel R; Kostyk E; Mazurczak T Med Wieku Rozwoj; 2009; 13(2):81-93. PubMed ID: 19837989 [TBL] [Abstract][Full Text] [Related]
22. Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea. Jang W; Kim Y; Han E; Park J; Chae H; Kwon A; Choi H; Kim J; Son JO; Lee SJ; Hong BY; Jang DH; Han JY; Lee JH; Kim SY; Lee IG; Sung IK; Moon Y; Kim M; Park JH Ann Lab Med; 2019 May; 39(3):299-310. PubMed ID: 30623622 [TBL] [Abstract][Full Text] [Related]
23. [Unbalanced subtelomic rearrangement involving 9q and 22q in a child with mental retardation and multiple congenital anomalies]. Xiao B; Xing Y; Ji X; Xu Y; Ni L; Zhu Y; Tao J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):666-9. PubMed ID: 24327143 [TBL] [Abstract][Full Text] [Related]
24. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization. Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833 [TBL] [Abstract][Full Text] [Related]
25. Genotype-Phenotype Analysis of 8q24.3 Duplication and 21q22.3 Deletion in a Chinese Patient and Literature Review. Sun H; Wan N Public Health Genomics; 2021; 24(5-6):218-228. PubMed ID: 34265769 [TBL] [Abstract][Full Text] [Related]
26. Familial 3-Way Balanced Translocation Causes 1q43→qter Loss and 10q25.2→qter Gain in a Severely Affected Male Toddler. Córdova-Fletes C; Arámbula-Meraz E; Zarazúa-Niño AI; Madueña-Molina J; Sáinz-Barraza ME; González-García JR; León-León C; López-López G; Lugo-Guzmán EG; Picos-Cárdenas VJ Cytogenet Genome Res; 2019; 157(4):231-238. PubMed ID: 30933949 [TBL] [Abstract][Full Text] [Related]
27. A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder. Casey JP; Goggin P; McDaid J; White M; Ennis S; Betts DR; Lucas JS; Elnazir B; Lynch SA BMC Med Genet; 2015 Jun; 16():45. PubMed ID: 26123568 [TBL] [Abstract][Full Text] [Related]
28. Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p. Oegema R; van Zutven LJ; van Hassel DA; Huijbregts GC; Hoogeboom AJ Eur J Med Genet; 2012 Apr; 55(4):265-8. PubMed ID: 22406089 [TBL] [Abstract][Full Text] [Related]
29. [Clinical genetic analysis of an infant with 1q21.3-qter duplication and Xpter-p11 deletion caused by maternal balanced chromosomal translocation]. Lin L; Zhao C; Lv Y; Zhao X; Li L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 May; 39(5):514-517. PubMed ID: 35598268 [TBL] [Abstract][Full Text] [Related]
30. Detection of an Underlying 22q11.2 Duplication in a Female Neonate With Trisomy 18. Turbiville DE; Wu H; Dong J Lab Med; 2017 Nov; 48(4):372-375. PubMed ID: 29036626 [TBL] [Abstract][Full Text] [Related]
31. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype. Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518 [TBL] [Abstract][Full Text] [Related]
32. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development. Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571 [TBL] [Abstract][Full Text] [Related]
33. Detection of an unbalanced t(4;15) by FISH in a child with multiple congenital anomalies. Celep F; Acar H; Aynaci O; Aynaci FM; Karagüzel A Genet Couns; 2001; 12(4):319-26. PubMed ID: 11837600 [TBL] [Abstract][Full Text] [Related]
34. [Phenotypic and genetic analysis of a pedigree with 4p16 microduplication and 8p23 microdeletion]. Li C; Hou R; Liu C; Li LJ; Lyu Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):989-992. PubMed ID: 31598942 [TBL] [Abstract][Full Text] [Related]
35. Cryptic subtelomeric translocations in the 22q13 deletion syndrome. Praphanphoj V; Goodman BK; Thomas GH; Raymond GV J Med Genet; 2000 Jan; 37(1):58-61. PubMed ID: 10633138 [TBL] [Abstract][Full Text] [Related]
36. Pure duplication of 19p13.3. Ishikawa A; Enomoto K; Tominaga M; Saito T; Nagai J; Furuya N; Ueno K; Ueda H; Masuno M; Kurosawa K Am J Med Genet A; 2013 Sep; 161A(9):2300-4. PubMed ID: 23897601 [TBL] [Abstract][Full Text] [Related]
37. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization]. Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946 [TBL] [Abstract][Full Text] [Related]
38. Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. Qiao Y; Bagheri H; Tang F; Badduke C; Martell S; Lewis SME; Robinson W; Connolly MB; Arbour L; Rajcan-Separovic E Eur J Med Genet; 2019 Feb; 62(2):103-108. PubMed ID: 29908350 [TBL] [Abstract][Full Text] [Related]
39. Xp22.3; Yq11.2 chromosome translocation and its clinical manifestations. Frints SG; Fryns J; Lagae L; Syrrou M; Marynen P; Devriendt K Ann Genet; 2001; 44(2):71-6. PubMed ID: 11522244 [TBL] [Abstract][Full Text] [Related]
40. Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor. Micale MA; Embrey B; Macknis JK; Harper CE; Aughton DJ Eur J Med Genet; 2016 Dec; 59(12):618-623. PubMed ID: 27794475 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]