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5. [Heteromorphism of chromosome 1, 9 and 16 homologs in persons living in regions differing in the level of longevity]. Kuznetsova SM; Zaritskaia MIu; Berdyshev GD Tsitol Genet; 1988; 22(4):27-32. PubMed ID: 2973673 [TBL] [Abstract][Full Text] [Related]
6. Euchromatic 16p+ heteromorphism: first report in North America. Jalal SM; Schneider NR; Kukolich MK; Wilson GN Am J Med Genet; 1990 Dec; 37(4):548-50. PubMed ID: 2260607 [TBL] [Abstract][Full Text] [Related]
7. Two extra euchromatic bands in the qh region of chromosome 9. Ozkinay F; Ercal D; Ozkinay C; Onay H; Bora E; Erler A Genet Couns; 2005; 16(1):45-8. PubMed ID: 15844778 [TBL] [Abstract][Full Text] [Related]
8. Chromosome imbalance, normal phenotype, and imprinting. Bortotto L; Piovan E; Furlan R; Rivera H; Zuffardi O J Med Genet; 1990 Sep; 27(9):582-7. PubMed ID: 2231652 [TBL] [Abstract][Full Text] [Related]
9. Extra euchromatic band in the qh region of chromosome 9. von Beust G; Bink K Fetal Diagn Ther; 1999; 14(1):35-7. PubMed ID: 10072648 [TBL] [Abstract][Full Text] [Related]
10. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up. Kim JJ; Rhee HS; Chung YT; Park SY; Choi SK Exp Mol Med; 1999 Sep; 31(3):134-6. PubMed ID: 10551261 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of a large centromeric heteromorphism of chromosome 12: implications for genetic counseling. Chantot-Bastaraud S; Siffroi JP; Berkane N; Heim N; Herve F; Uzan S; Vendrely E Fetal Diagn Ther; 2003; 18(2):111-3. PubMed ID: 12576746 [TBL] [Abstract][Full Text] [Related]
12. [Cytogenetic study of a family with 15p+ chromosomal plymorphism]. Manzanal Martínez AI; Robledo Batanero M; Ramos Corrales C; Ayuso García C; Sánchez Cascos A An Esp Pediatr; 1992 Apr; 36(4):269-71. PubMed ID: 1605408 [TBL] [Abstract][Full Text] [Related]
13. Euchromatic variant 16p+. Implications in prenatal diagnosis. López Pajares I; Villa O; Salido M; Mori MA; Gonzalez A; Lapunzina P; De Torres ML; Vallcorba I; Palomares M; Fernández L; Delicado A Prenat Diagn; 2006 Jun; 26(6):535-8. PubMed ID: 16634122 [TBL] [Abstract][Full Text] [Related]
14. Interstitial deletions without phenotypic effect: prenatal diagnosis of a new family and brief review. Barber JC; Mahl H; Portch J; Crawfurd MD Prenat Diagn; 1991 Jun; 11(6):411-6. PubMed ID: 1924182 [TBL] [Abstract][Full Text] [Related]
15. Familial occurrence of cancer and heteromorphism of the heterochromatic segment of chromosome 1. Köpf I; Islam MQ; Friberg LG; Levan G Hereditas; 1989; 110(1):79-83. PubMed ID: 2777631 [TBL] [Abstract][Full Text] [Related]
16. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance. Barber JC; Joyce CA; Collinson MN; Nicholson JC; Willatt LR; Dyson HM; Bateman MS; Green AJ; Yates JR; Dennis NR J Med Genet; 1998 Jun; 35(6):491-6. PubMed ID: 9643291 [TBL] [Abstract][Full Text] [Related]
17. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization. Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of a large heteromorphic region in a chromosome 5: implications for genetic counseling. Fineman RM; Issa B; Weinblatt V Am J Med Genet; 1989 Apr; 32(4):498-9. PubMed ID: 2773992 [TBL] [Abstract][Full Text] [Related]
19. Duplication of chromosome region 8p23.1-->p23.3: a benign variant? Engelen JJ; Moog U; Evers JL; Dassen H; Albrechts JC; Hamers AJ Am J Med Genet; 2000 Mar; 91(1):18-21. PubMed ID: 10751083 [TBL] [Abstract][Full Text] [Related]
20. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q. Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]