158 related articles for article (PubMed ID: 30166997)
1. Recombinant chromosome 4 in two fetuses - case report and literature review.
Wu Y; Wang Y; Wen SW; Zhao X; Hu W; Liu C; Gao L; Zhang Y; Wang S; Yang X; He B; Cheng W
Mol Cytogenet; 2018; 11():48. PubMed ID: 30166997
[TBL] [Abstract][Full Text] [Related]
2. A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
Dufke A; Eggermann K; Balg S; Stengel-Rutkowski S; Enders H; Kaiser P
Cytogenet Cell Genet; 2000; 91(1-4):85-9. PubMed ID: 11173836
[TBL] [Abstract][Full Text] [Related]
3. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
Battaglia A; Brothman AR; Carey JC
Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
[TBL] [Abstract][Full Text] [Related]
4. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
Hirsch B; Baldinger S
Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
[TBL] [Abstract][Full Text] [Related]
5. Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review.
Hemmat M; Hemmat O; Anguiano A; Boyar FZ; El Naggar M; Wang JC; Wang BT; Sahoo T; Owen R; Haddadin M
Mol Cytogenet; 2013 May; 6(1):17. PubMed ID: 23639048
[TBL] [Abstract][Full Text] [Related]
6. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
7. Recombinant chromosome 4 resulting from a maternal pericentric inversion in two sisters presenting consistent dysmorphic features.
Stembalska A; Laczmanska I; Schlade-Bartusiak K; Czemarmazowicz H; Murawski M; Sasiadek M
Eur J Pediatr; 2007 Jan; 166(1):67-71. PubMed ID: 17013597
[TBL] [Abstract][Full Text] [Related]
8. [Recombinant chromosome 4 with partial 4p deletion and 4q duplication inherited from paternal pericentric inversion].
Mun SJ; Cho EH; Chey MJ; Shim GH; Shin BM; Lee RK; Ko JK; Yoo SJ
Korean J Lab Med; 2010 Feb; 30(1):89-92. PubMed ID: 20197729
[TBL] [Abstract][Full Text] [Related]
9. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
Garcia-Heras J; Martin J
Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
[TBL] [Abstract][Full Text] [Related]
11. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
[TBL] [Abstract][Full Text] [Related]
12. Recombinant Down syndrome: a case report and literature review.
Lazzaro SJ; Speevak MD; Farrell SA
Clin Genet; 2001 Feb; 59(2):128-30. PubMed ID: 11260215
[TBL] [Abstract][Full Text] [Related]
13. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity.
Aslan H; Karaca N; Basaran S; Ermis H; Ceylan Y
BMC Pregnancy Childbirth; 2003 Jan; 3(1):1. PubMed ID: 12546710
[TBL] [Abstract][Full Text] [Related]
15. Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature.
Habhab W; Mau-Holzmann U; Singer S; Rieß A; Kagan KO; Gerbig I; Schäferhoff K; Dufke A; Kehrer M
Am J Med Genet A; 2020 Nov; 182(11):2680-2684. PubMed ID: 32803851
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents.
Tassano E; Alpigiani MG; Salvati P; Gimelli S; Lorini R; Gimelli G
Gene; 2012 Dec; 511(2):338-40. PubMed ID: 23031810
[TBL] [Abstract][Full Text] [Related]
18. Pericentric inversions of chromosome 4: report of a new family and review of the literature.
Villa A; Urioste M; Carrascosa MC; Vázquez S; Martínez A; Martínez-Frías ML
Clin Genet; 1995 Nov; 48(5):255-60. PubMed ID: 8825604
[TBL] [Abstract][Full Text] [Related]
19. Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome.
Paskulin GA; Riegel M; Cotter PD; Kiss A; Rosa RF; Zen PR; Mombach R; Graziadio C
Am J Med Genet A; 2009 Jun; 149A(6):1302-7. PubMed ID: 19449429
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy.
Chen CP
Taiwan J Obstet Gynecol; 2007 Dec; 46(4):336-51. PubMed ID: 18182339
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]