127 related articles for article (PubMed ID: 31951340)
1. 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]
2. New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.
Serra G; Antona V; Cimador M; Collodoro G; Guida M; Piro E; Schierz IAM; Verde V; Giuffrè M; Corsello G
Ital J Pediatr; 2023 Feb; 49(1):17. PubMed ID: 36759911
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype.
Dundar M; Uzak A; Erdogan M; Saatci C; Akdeniz S; Luleci G; Keser I; Karauzum S
Genet Couns; 2011; 22(2):199-205. PubMed ID: 21848013
[TBL] [Abstract][Full Text] [Related]
4. Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2.
Dworschak GC; Crétolle C; Hilger A; Engels H; Korsch E; Reutter H; Ludwig M
Clin Genet; 2017 May; 91(5):661-671. PubMed ID: 27549440
[TBL] [Abstract][Full Text] [Related]
5. Multiple congenital malformations including severe eye anomalies and abnormal cerebellar development with Dandy-Walker malformation in a girl with partial trisomy 3q.
de Azevedo Moreira LM; Neri FB; de Quadros Uzeda S; de Carvalho AF; Santana GC; Souza FR; Rollemberg JC
Ophthalmic Genet; 2005 Mar; 26(1):37-43. PubMed ID: 15823924
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Bilateral anterior segment dysgenesis in an infant with partial trisomy 16q and partial monosomy 3p.
Dikmetas O; Simsek Kiper PO; Mocan MC; Utine EG; Boduroglu K; Irkec M
J AAPOS; 2012 Oct; 16(5):473-5. PubMed ID: 23084388
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Partial duplication of 3q and distal deletion of 10q inherited from a maternal balanced translocation.
Su PH; Chen JY; Chen SJ; Hung HM
J Formos Med Assoc; 2004 Nov; 103(11):853-7. PubMed ID: 15549153
[TBL] [Abstract][Full Text] [Related]
13. [Prenatal diagnosis of partial trisomy 3q in a fetus].
Su N; Lou G; Wang H; Hao B; Liao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug; 36(8):813-816. PubMed ID: 31400135
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy 3q causing mild Cornelia de Lange phenotype.
Holder SE; Grimsley LM; Palmer RW; Butler LJ; Baraitser M
J Med Genet; 1994 Feb; 31(2):150-2. PubMed ID: 8182724
[TBL] [Abstract][Full Text] [Related]
15. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
Ayral D; Raudrant D; Charleux JP; Noel B
Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
[TBL] [Abstract][Full Text] [Related]
16. Chromosomes in the Cornelia de Lange syndrome.
Beck B; Mikkelsen M
Hum Genet; 1981; 59(4):271-6. PubMed ID: 7333580
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23).
Tranebjaerg L; Baekmark UB; Dyhr-Nielsen M; Kreiborg S
Clin Genet; 1987 Aug; 32(2):137-43. PubMed ID: 3652493
[TBL] [Abstract][Full Text] [Related]
19. Partial trisomy of chromosome 3 (3q12 leads to qter) owing to 3q/18p translocation. A trisomy 3q syndrome.
Salazar D; Rosenfeld W; Verma RS; Jhaveri RC; Dosik H
Am J Dis Child; 1979 Oct; 133(10):1006-8. PubMed ID: 495588
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia.
Jung SH; Shim SH; Park SH; Park JE; Park HR; Ahn EH; Kim SH; Cha DH
Gene; 2012 May; 498(2):237-41. PubMed ID: 22366303
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
