147 related articles for article (PubMed ID: 24669257)
21. Partial proximal trisomy 10q syndrome: a new case.
Nucaro A; Faedda A; Cao A; Boccone L
Genet Couns; 2002; 13(4):411-6. PubMed ID: 12558111
[TBL] [Abstract][Full Text] [Related]
22. De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature.
Bartolini L; Sartori S; Lenzini E; Rigon C; Cainelli E; Agrati C; Toldo I; Donà M; Trevisson E
Gene; 2013 Jul; 524(2):368-72. PubMed ID: 23612255
[TBL] [Abstract][Full Text] [Related]
23. [17p13.3 duplication as a cause of psychomotor developmental delay in an infant - a further case of a new syndrome].
Przybylska-Kruszewska A; Kutkowska-Kaźmierczak A; Krzywdzińska A; Smyk M; Nowakowska B; Gryglicka H; Obersztyn E; Hozyasz KK
Pol Merkur Lekarski; 2016 Apr; 40(238):255-9. PubMed ID: 27137828
[TBL] [Abstract][Full Text] [Related]
24. Report on 3 patients with 12p duplication including GRIN2B.
Poirsier C; Landais E; Bednarek N; Nobecourt JM; Khoury M; Schmidt P; Morville P; Gruson N; Clomes S; Michel N; Riot A; Manjeongean C; Gaillard D; Doco-Fenzy M
Eur J Med Genet; 2014 Apr; 57(5):185-94. PubMed ID: 24503147
[TBL] [Abstract][Full Text] [Related]
25. De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.
Debost-Legrand A; Capri Y; Gouas L; Pebrel-Richard C; Veronese L; Tchirkov A; Haoud K; Boespflug-Tanguy O; Goumy C; Vago P
Pathol Biol (Paris); 2011 Dec; 59(6):309-13. PubMed ID: 21145667
[TBL] [Abstract][Full Text] [Related]
26. Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
Sarri C; Douzgou S; Gyftodimou Y; Tümer Z; Ravn K; Pasparaki A; Sarafidou T; Kontos H; Kokotas H; Karadima G; Grigoriadou M; Pandelia E; Theodorou V; Moschonas NK; Petersen MB
Am J Med Genet A; 2011 Nov; 155A(11):2841-54. PubMed ID: 21964744
[TBL] [Abstract][Full Text] [Related]
27. The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability.
Ha K; Shen Y; Graves T; Kim CH; Kim HG
Mol Cytogenet; 2016; 9():74. PubMed ID: 27708714
[TBL] [Abstract][Full Text] [Related]
28. Partial trisomy 10q in three unrelated patients.
Taysi K; Yang V; Monaghan N; Beraha N
Ann Genet; 1983; 26(2):79-85. PubMed ID: 6604490
[TBL] [Abstract][Full Text] [Related]
29. Characterization of a de novo sSMC 17 detected in a girl with developmental delay and dysmorphic features.
Stavber L; Bertok S; Kovač J; Volk M; Lovrečić L; Battelino T; Hovnik T
Mol Cytogenet; 2017; 10():10. PubMed ID: 28344653
[TBL] [Abstract][Full Text] [Related]
30. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
Schaeffer AJ; Chung J; Heretis K; Wong A; Ledbetter DH; Lese Martin C
Am J Hum Genet; 2004 Jun; 74(6):1168-74. PubMed ID: 15127362
[TBL] [Abstract][Full Text] [Related]
31. A Patient with Trisomy 4p and Monosomy 10q.
Sobhani M; Tahmasbi P; Nasiri F; Rahnama M; Karimi-Nejad R; Tabatabaiefar MA
Arch Iran Med; 2019 Jul; 22(7):414-417. PubMed ID: 31679386
[TBL] [Abstract][Full Text] [Related]
32. Clinical, cytogenetic and molecular-cytogenetic characterization of a patient with a de novo tandem proximal-intermediate duplication of 16q and review of the literature.
Lonardo F; Perone L; Maioli M; Ciavarella M; Ciccone R; Monica MD; Lombardi C; Forino L; Cantalupo G; Masella L; Scarano F
Am J Med Genet A; 2011 Apr; 155A(4):769-77. PubMed ID: 21416588
[TBL] [Abstract][Full Text] [Related]
33. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
34. Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features.
Dhangar S; Korgaonkar S; Vundinti BR
Intractable Rare Dis Res; 2019 Feb; 8(1):72-77. PubMed ID: 30881863
[TBL] [Abstract][Full Text] [Related]
35. Partial proximal 10q trisomy: a new case associated with biliary atresia.
Lysy PA; Sibille C; Gillerot Y; Smets F; Sokal EM
Hereditas; 2007 Nov; 144(5):191-4. PubMed ID: 18031353
[TBL] [Abstract][Full Text] [Related]
36. Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.
Manolakos E; Sarri C; Vetro A; Kefalas K; Leze E; Sofocleus C; Kitsos G; Merou K; Kokotas H; Papadopoulou A; Attilakos A; Petersen MB; Kitsiou-Tzeli S
Mol Cytogenet; 2011 Feb; 4(1):6. PubMed ID: 21345209
[TBL] [Abstract][Full Text] [Related]
37. A triplication of the Williams-Beuren syndrome region in a patient with mental retardation, a severe expressive language delay, behavioural problems and dysmorphisms.
Beunders G; van de Kamp JM; Veenhoven RH; van Hagen JM; Nieuwint AW; Sistermans EA
J Med Genet; 2010 Apr; 47(4):271-5. PubMed ID: 19752158
[TBL] [Abstract][Full Text] [Related]
38. Pure Interstitial 7q21.3-q 31.1 Duplication: A Rare Segmental Genomic Aneuploidy: Case Report and Review of Cases with Distal and Similar Segment Involved.
Di Nora A; Lena G; Giugno A; Di Mari A; Smilari P; Minardi C; Pavone P
Glob Med Genet; 2021 Sep; 8(3):123-128. PubMed ID: 34430965
[TBL] [Abstract][Full Text] [Related]
39. 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; 155A(7):1735-9. PubMed ID: 21626676
[TBL] [Abstract][Full Text] [Related]
40. The first patient with tandem duplication of 6q14q16: Molecular and phenotypic characterization.
Sanmann JN; Casas KA; Bevilacqua J; Bishay DL; Clark T; Van Dyke AZ; Leiferman PC; Reddi HV; Starr LJ
Am J Med Genet A; 2016 Sep; 170(9):2416-20. PubMed ID: 27338032
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
