266 related articles for article (PubMed ID: 6609673)
1. Interstitial deletion of long arm of chromosome 13.
Carnevale A; Frias S; Alcantar R
Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673
[TBL] [Abstract][Full Text] [Related]
2. Long arm deletion of chromosome 13 with exclusion of esterase D from 13q32 leads to 13qter.
Telfer MA; Clark CE; Casey PA; Cowell HR; Stroud HH
Clin Genet; 1980 Jun; 17(6):428-32. PubMed ID: 7398115
[TBL] [Abstract][Full Text] [Related]
3. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
4. Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth.
Balci S; Yuksel Konuk B; Atik F; Oguz AK; Ergun MA; Baltaci V; Kosyakova N; Liehr T
Genet Couns; 2010; 21(3):317-24. PubMed ID: 20964123
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
[TBL] [Abstract][Full Text] [Related]
6. 7q deletion syndrome (7q32 leads to 7qter).
Harris EL; Wappner RS; Palmer CG; Hall B; Dinno N; Seashore MR; Breg WR
Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
[TBL] [Abstract][Full Text] [Related]
7. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
[TBL] [Abstract][Full Text] [Related]
8. Langer-Giedion syndrome with interstitial 8q-deletion.
Zabel BU; Baumann WA
Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
[TBL] [Abstract][Full Text] [Related]
9. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
Back E; Hertel C; Vogel W; Bettecken F; Thiesen M
Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761
[TBL] [Abstract][Full Text] [Related]
10. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE
Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660
[TBL] [Abstract][Full Text] [Related]
11. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
Zaletaev DV; Dadali EL; Kuleshov NP
Tsitol Genet; 1987; 21(3):213-6. PubMed ID: 3617217
[TBL] [Abstract][Full Text] [Related]
12. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
Copelli S; del Rey G; Heinrich J; Coco R
Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
[TBL] [Abstract][Full Text] [Related]
13. A specific syndrome due to deletion of the distal long arm of chromosome 1.
Meinecke P; Vögtel D
Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
[TBL] [Abstract][Full Text] [Related]
14. [Interstitial deletion of the long arms of chromosome 13].
Molina M; Santolaya JM; Onaindía ML; Sánchez E; De Gárate J
An Esp Pediatr; 1982 Apr; 16(4):346-51. PubMed ID: 7125394
[TBL] [Abstract][Full Text] [Related]
15. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
Wilson MG; Towner JW; Forsman I; Siris E
Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
[TBL] [Abstract][Full Text] [Related]
16. Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.
Keppen LD; Gollin SM; Edwards D; Sawyer J; Wilson W; Overhauser J
Am J Med Genet; 1992 Oct; 44(3):356-60. PubMed ID: 1488985
[TBL] [Abstract][Full Text] [Related]
17. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases.
Young RS; Weaver DD; Kukolich MK; Heerema NA; Palmer CG; Kawira EL; Bender HA
Am J Med Genet; 1984 Feb; 17(2):437-50. PubMed ID: 6199974
[TBL] [Abstract][Full Text] [Related]
18. A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter).
Lukusa T; Devriendt K; Fryns JP
Ann Genet; 1999; 42(2):91-4. PubMed ID: 10434122
[TBL] [Abstract][Full Text] [Related]
19. Interstitial del(13q) associated with blindness and mental retardation.
Juberg RC; Mowrey PN
Am J Med Genet; 1984 Mar; 17(3):609-13. PubMed ID: 6711612
[TBL] [Abstract][Full Text] [Related]
20. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
Narahara K; Kikkawa K; Murakami M; Hiramoto K; Namba H; Tsuji K; Yokoyama Y; Kimoto H
Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
