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2. Prenatal detection of pericentric inversion of chromosome 12. Kim HJ; Levy J; Reguero W; Iu B; Wallach RC Diagn Gynecol Obstet; 1980; 2(3):231-4. PubMed ID: 7439022 [TBL] [Abstract][Full Text] [Related]
3. [Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]]. Baumann W; Zabel B; Holl M Ann Genet; 1984; 27(2):106-8. PubMed ID: 6331785 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. The prenatal detection of a familial pericentric inversion of chromosome 19. Couzin DA; Watt JL; Stephen GS Prenat Diagn; 1986; 6(1):79-82. PubMed ID: 3952061 [TBL] [Abstract][Full Text] [Related]
6. A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling. Ridler MA; Sutton SD Prenat Diagn; 1981 Jan; 1(1):81-4. PubMed ID: 7346813 [TBL] [Abstract][Full Text] [Related]
7. Inversion of chromosome 2 (p11p13): frequency and implications for genetic counselling. MacDonald IM; Cox DM Hum Genet; 1985; 69(3):281-3. PubMed ID: 3980020 [TBL] [Abstract][Full Text] [Related]
8. Karyotypic evolution in acute myelomonocytic leukemia with pericentric inversion of chromosome 16. Taniwaki M; Inazawa J; Horiike S; Misawa S; Abe T; Takino T Cancer Genet Cytogenet; 1987 Feb; 24(2):257-62. PubMed ID: 3466677 [TBL] [Abstract][Full Text] [Related]
9. Inv(10)(p11.2q21.2), a variant chromosome. Collinson MN; Fisher AM; Walker J; Currie J; Williams L; Roberts P Hum Genet; 1997 Dec; 101(2):175-80. PubMed ID: 9402964 [TBL] [Abstract][Full Text] [Related]
10. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature. Hales HA; Peterson CM; Carey J; Hecht BK; Hecht F Am J Med Genet; 1993 Nov; 47(6):848-51. PubMed ID: 8279482 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Prenatal diagnosis of pericentric inversion of chromosome No. 17 in a twin pregnancy. Kassam G; Chen AT; Goldberg MF; Trusler S; Oakley GP Prenat Diagn; 1984; 4(3):213-6. PubMed ID: 6463028 [TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of a 46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat. Varela M; Wang N; Cerrillo M Hum Genet; 1987 Jan; 75(1):93-4. PubMed ID: 3804337 [TBL] [Abstract][Full Text] [Related]
15. Detection of pericentric inversion of X chromosome in a male fetus. Wenger SL; Cutenese C; Brancazio LR Am J Med Genet; 1999 Dec; 87(4):339-41. PubMed ID: 10588841 [TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of pericentric inversion in homologues of chromosome 9: a decision dilemma. Sharony R; Amiel A; Einy R; Fejgin M Am J Perinatol; 2007 Feb; 24(2):137-40. PubMed ID: 17304418 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of inv(X)(q12q28) in a male fetus. Neu RL; Brar HS; Koos BJ J Med Genet; 1988 Jan; 25(1):52-3. PubMed ID: 3351892 [TBL] [Abstract][Full Text] [Related]
19. Prenatal detection of an inverted X chromosome in a male. Brothman AR; Newlin A; Phillips SE; Kinzie GQ; Leichtman LG Clin Genet; 1993 Sep; 44(3):139-41. PubMed ID: 8275571 [TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement. Bogart MH; Bradshaw CL; Jones OW; Schanberger JE J Med Genet; 1986 Apr; 23(2):180-3. PubMed ID: 3712398 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]