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23. Rieger's syndrome with pericentric inversion of chromosome 6. Heinemann MH; Breg R; Cotlier E Br J Ophthalmol; 1979 Jan; 63(1):40-4. PubMed ID: 760775 [TBL] [Abstract][Full Text] [Related]
24. Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 leads to 14qter). Trunca C; Opitz JM Am J Med Genet; 1977; 1(2):217-28. PubMed ID: 610431 [TBL] [Abstract][Full Text] [Related]
26. Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion. Hoo JJ; Lorenz R; Fischer A; Fuhrmann W Hum Genet; 1982; 62(2):113-6. PubMed ID: 7160842 [TBL] [Abstract][Full Text] [Related]
27. A new pericentric inversion of chromosome 6 in an abnormal infant. Duckett DP; Roberts SH Ann Genet; 1980; 23(2):117-8. PubMed ID: 6967284 [TBL] [Abstract][Full Text] [Related]
28. Unusual chromosome aberrations in 3 children with Down syndrome. Osztovics M; Tóth S; Wilhelm O Acta Paediatr Acad Sci Hung; 1982; 23(3):283-9. PubMed ID: 6217717 [TBL] [Abstract][Full Text] [Related]
30. Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants? Moedjono SJ; Sparkes RS Ann Genet; 1980; 23(4):235-7. PubMed ID: 6971603 [TBL] [Abstract][Full Text] [Related]
31. Fetal anomalies associated with an inversion duplication 13 chromosome. Rijhsinghani AG; Hruban RH; Stetten G Obstet Gynecol; 1988 Jun; 71(6 Pt 2):991-4. PubMed ID: 3287254 [TBL] [Abstract][Full Text] [Related]
32. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families. Boué J; Taillemite JL; Hazael-Massieux P; Léonard C; Boué A Humangenetik; 1975 Sep; 30(3):217-24. PubMed ID: 1184007 [TBL] [Abstract][Full Text] [Related]
33. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q. Verma RS; Dosik H; Wexler IB J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332 [TBL] [Abstract][Full Text] [Related]
34. 46,XY/47,XYY/48,XYYY karyotype in a 3-year-old boy ascertained because of radioulnar synostosis. James C; Robson L; Jackson J; Smith A Am J Med Genet; 1995 May; 56(4):389-92. PubMed ID: 7604847 [TBL] [Abstract][Full Text] [Related]
35. A familial paracentric inv(1)(q42q44) resulting in a child with a del(1)(q42) karyotype. Speevak M; Hunter AG; Hughes H; Cox DM Ann Genet; 1985; 28(3):177-80. PubMed ID: 3879153 [TBL] [Abstract][Full Text] [Related]
36. A long unidentifiable extra chromosomal segment--a possible duplication of human 7q. Wahrman J; Cohen MM; Rosenmann A; Goitein R; Richler C; Dagan J Cytogenet Cell Genet; 1978; 20(1-6):160-8. PubMed ID: 648175 [TBL] [Abstract][Full Text] [Related]
37. A 13;13 tandem chromosome translocation in a subject with congenital anomalies. Repository identification No. GM-2018. Kohn G; Cohen MM; Aronson MM; Greene AE; Coriell LL Cytogenet Cell Genet; 1979; 24(1):72. PubMed ID: 456042 [No Abstract] [Full Text] [Related]
38. [Pericentric inversion of chromosome 9 in two women with developmental defects of the internal genitalia]. Kirillova EA; Rozovskiĭ IS; Kurbanova AG; Karetnikova NA Tsitol Genet; 1979; 13(4):300-4. PubMed ID: 516157 [No Abstract] [Full Text] [Related]
39. Chromosome 6/15 translocation with multiple congenital anomalies. Ming PM; Goodner DM; Park TS Obstet Gynecol; 1977 Feb; 49(2):251-3. PubMed ID: 834413 [TBL] [Abstract][Full Text] [Related]