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6. Transmission of a ring chromosome 18 from a mother with 46,XX/47,XX, + r(18) mosaicism to her daughter, resulting in a 46,XX,r(18) karyotype. Jenderny J; Caliebe A; Beyer C; Grote W J Med Genet; 1993 Nov; 30(11):964-5. PubMed ID: 8301656 [TBL] [Abstract][Full Text] [Related]
8. Three cases of ring chromosome 2, one derived from a paternal 2/6 translocation. Maraschio P; Danesino C; Garau A; Saputo V; Vigi V; Volpato S Hum Genet; 1979 Apr; 48(2):157-67. PubMed ID: 457140 [TBL] [Abstract][Full Text] [Related]
9. Ring chromosome 15 in a patient with features of Fryns' syndrome. de Jong G; Rossouw RA; Retief AE J Med Genet; 1989 Jul; 26(7):469-70. PubMed ID: 2746621 [TBL] [Abstract][Full Text] [Related]
10. MULTIPLE CONGENITAL ANOMALIES ASSOCIATED WITH A PARTIALLY RING-SHAPED CHROMOSOME PROBABLY DERIVED FROM CHROMOSOME NO. 18 IN MAN. GROPP A; JUSSEN A; OFTERINGER K Nature; 1964 May; 202():829-30. PubMed ID: 14187649 [No Abstract] [Full Text] [Related]
11. Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3. Roberts SH; Hughes HE; Davies SJ; Meredith AL J Med Genet; 1991 Jul; 28(7):479-81. PubMed ID: 1895319 [TBL] [Abstract][Full Text] [Related]
12. A patient with ring 9 chromosome 46,XY,r(9)(p24.1q34.3). Kasa N; Kasai R Acta Paediatr Jpn; 1988 Dec; 30(6):710-3. PubMed ID: 3149132 [No Abstract] [Full Text] [Related]
13. Ring (13),t(2;6) associated with familial fragile (16). Ventruto V; Rinaldi A; Renda S; Stabile M; Rinaldi MM; Cavaliere ML; Conte N; Aveta V J Med Genet; 1984 Jun; 21(3):233. PubMed ID: 6748026 [No Abstract] [Full Text] [Related]
14. Deletion of the short arm of chromosome 2 from a subject with congenital anomalies. Repository identification no. GM-1138. Zackai E; Emanuel B; Mellman WJ; Aronson MM; Bozarth B; Greene AE; Coriell LL Cytogenet Cell Genet; 1977; 18(2):108. PubMed ID: 862431 [No Abstract] [Full Text] [Related]
15. Interstitial deletion and ring chromosome derived from 16q. Krauss CM; Caldwell D; Atkins L J Med Genet; 1987 May; 24(5):308-12. PubMed ID: 3585948 [TBL] [Abstract][Full Text] [Related]
16. Ring chromosome 2 in a child with growth failure and few congenital abnormalities. Vigfusson NV; Kapstafer KJ; Lloyd MA Am J Med Genet; 1980; 7(3):383-9. PubMed ID: 7468662 [TBL] [Abstract][Full Text] [Related]
17. Holoprosencephaly associated with ring chromosome 21. Hoovers JM; Jansweijer MC Clin Genet; 1987 Sep; 32(3):207. PubMed ID: 3621668 [No Abstract] [Full Text] [Related]
18. Aniridia, congenital glaucoma, and hydrocephalus in a male infant with ring chromosome 6. Levin H; Ritch R; Barathur R; Dunn MW; Teekhasaenee C; Margolis S Am J Med Genet; 1986 Oct; 25(2):281-7. PubMed ID: 3777023 [TBL] [Abstract][Full Text] [Related]
20. Another case of ring chromosome 9 associated with gastroesophageal reflux. Manouvrier-Hanu S; Turck D; Farriaux JP Am J Med Genet; 1989 Apr; 32(4):558. PubMed ID: 2774007 [No Abstract] [Full Text] [Related] [Next] [New Search]