94 related articles for article (PubMed ID: 24551980)
1. A case of dup(3q) syndrome.
Koç A; Ekmekci AY; Ozer O
Genet Couns; 2013; 24(4):381-5. PubMed ID: 24551980
[TBL] [Abstract][Full Text] [Related]
2. Novel case of dup(3q) syndrome due to a de novo interstitial duplication 3q24-q26.31 with minimal overlap to the dup(3q) critical region.
Meins M; Hagh JK; Gerresheim F; Einhoff E; Olschewski H; Strehl H; Epplen JT
Am J Med Genet A; 2005 Jan; 132A(1):84-9. PubMed ID: 15551338
[TBL] [Abstract][Full Text] [Related]
3. Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
Rizzu P; Haddad BR; Vallcorba I; Alonso A; Ferro MT; Garcia-Sagredo JM; Baldini A
Am J Med Genet; 1997 Feb; 68(4):428-32. PubMed ID: 9021016
[TBL] [Abstract][Full Text] [Related]
4. A girl with inverted triplication of chromosome 3q25.3 --> q29 and multiple congenital anomalies consistent with 3q duplication syndrome.
Ounap K; Ilus T; Bartsch O
Am J Med Genet A; 2005 May; 134(4):434-8. PubMed ID: 15793836
[TBL] [Abstract][Full Text] [Related]
5. A new case of dup(3q) syndrome due to a pure duplication of 3qter.
Faas BH; De Vries BB; Van Es-Van Gaal J; Merkx G; Draaisma JM; Smeets DF
Clin Genet; 2002 Oct; 62(4):315-20. PubMed ID: 12372060
[TBL] [Abstract][Full Text] [Related]
6. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
[TBL] [Abstract][Full Text] [Related]
7. Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.
van Essen AJ; Kok K; van den Berg A; de Jong B; Stellink F; Bos AF; Scheffer H; Buys CH
Hum Genet; 1991 Jun; 87(2):151-4. PubMed ID: 2066102
[TBL] [Abstract][Full Text] [Related]
8. Duplication 3q syndrome: molecular delineation of the critical region.
Aqua MS; Rizzu P; Lindsay EA; Shaffer LG; Zackai EH; Overhauser J; Baldini A
Am J Med Genet; 1995 Jan; 55(1):33-7. PubMed ID: 7702094
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial disease in 22q13 duplication syndrome.
Frye RE
J Child Neurol; 2012 Jul; 27(7):942-9. PubMed ID: 22378673
[TBL] [Abstract][Full Text] [Related]
10. Prenatal identification of partial 3q duplication syndrome.
Pasińska M; Adamczak R; Repczyńska A; Łazarczyk E; Iskra B; Runge AK; Haus O
BMC Med Genomics; 2019 Jun; 12(1):85. PubMed ID: 31196198
[TBL] [Abstract][Full Text] [Related]
11. A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review.
Pavone P; Praticò AD; Falsaperla R; Ruggieri M; Neri G; Pavone V; Zollino M
Clin Dysmorphol; 2016 Jul; 25(3):121-7. PubMed ID: 26918294
[No Abstract] [Full Text] [Related]
12. Further delineation of the dup(3q) syndrome.
Wilson GN; Dasouki M; Barr M
Am J Med Genet; 1985 Sep; 22(1):117-23. PubMed ID: 4050847
[TBL] [Abstract][Full Text] [Related]
13. Siblings with opposite chromosome constitutions, dup(2q)/del(7q) and del(2q)/dup(7q).
Shim SH; Shim JS; Min K; Lee HS; Park JE; Park SH; Hwang E; Kim M
Gene; 2014 Jan; 534(1):100-6. PubMed ID: 24095776
[TBL] [Abstract][Full Text] [Related]
14. A rare chromosomal disorder in a newborn: Trisomy 3q.
Kahvecioğlu D; Tatar-Aksoy H; Yıldız E; Bakır A; Alioğlu B
Turk J Pediatr; 2019; 61(2):271-274. PubMed ID: 31951340
[TBL] [Abstract][Full Text] [Related]
15. 3q29 microduplication syndrome: Clinical and molecular description of eleven new cases.
Coyan AG; Dyer LM
Eur J Med Genet; 2020 Dec; 63(12):104083. PubMed ID: 33039685
[TBL] [Abstract][Full Text] [Related]
16. Pure duplication 21q21.2-->qter due to a rea(21) in a Down syndrome girl. Remarks on nomenclature.
Dominguez MG; Arteaga-Alcaraz G; Rivera H
Genet Couns; 2012; 23(2):313-8. PubMed ID: 22876592
[TBL] [Abstract][Full Text] [Related]
17. Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia.
Ben-Abdallah-Bouhjar I; Hannachi H; Labalme A; Gmidène A; Mougou S; Soyah N; Gribaa M; Sanlaville D; Elghezal H; Saad A
Eur J Med Genet; 2012; 55(8-9):461-5. PubMed ID: 22683462
[TBL] [Abstract][Full Text] [Related]
18. Clinical, cytogenetic and molecular study in a case of r(3) with 3p deletion and review of the literature.
Guilherme RS; Bragagnolo S; Pellegrino R; Christofolini DM; Takeno SS; Carvolheira GM; Kulikowski LD; Melaragno MI
Cytogenet Genome Res; 2011; 134(4):325-30. PubMed ID: 21849783
[TBL] [Abstract][Full Text] [Related]
19. Acute myeloid leukemia presenting in a mother and daughter pair with the identical acquired karyotypic abnormality consisting of inversion 3q21q26 and monosomy 7: a review of possible mechanisms.
Lawrie A; Stevenson DA; Doig TN; Vickers MA; Culligan DJ
Cancer Genet; 2012 Nov; 205(11):599-602. PubMed ID: 23064135
[TBL] [Abstract][Full Text] [Related]
20. Identification of a putative regulatory subunit of a calcium-activated potassium channel in the dup(3q) syndrome region and a related sequence on 22q11.2.
Riazi MA; Brinkman-Mills P; Johnson A; Naylor SL; Minoshima S; Shimizu N; Baldini A; McDermid HE
Genomics; 1999 Nov; 62(1):90-4. PubMed ID: 10585773
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
