178 related articles for article (PubMed ID: 500091)
1. Presumptive long arm deletion of chromosome 8: a new syndrome?
Taysi K; Noetzel MJ; Strauss AW
Hum Genet; 1979 Sep; 51(1):49-53. PubMed ID: 500091
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).
Fryns JP; Logghe N; Van Eygen M; Van Der Berghe H
Hum Genet; 1979 Apr; 48(1):127-30. PubMed ID: 457127
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Interstitial deletion of the long arm of one 11 chromosome].
Taillemite JL; Morlier BG; Roux C
Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
[TBL] [Abstract][Full Text] [Related]
5. Developmental abnormalities associated with long arm deletion of chromosome No. 6.
Bartoshesky L; Lewis MB; Pashayan HM
Clin Genet; 1978 Jan; 13(1):68-71. PubMed ID: 624189
[TBL] [Abstract][Full Text] [Related]
6. Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome.
Rivera H; Rodríguez RM; Plascencia ML; Martínez y Martínez R; Nazara Z; Cantu JM
J Genet Hum; 1983 Dec; 31 Suppl 5():413-8. PubMed ID: 6674417
[TBL] [Abstract][Full Text] [Related]
7. Distal deletion of the short arm of chromosome No. 10: a case report.
Oka S; Nakano H; Yokochi T; Ueda K; Saito A
Jinrui Idengaku Zasshi; 1983 Dec; 28(4):291-6. PubMed ID: 6678316
[No Abstract] [Full Text] [Related]
8. Interstitial deletion for a region in the long arm of chromosome 16.
Lin CC; Lowry RB; Snyder FF
Hum Genet; 1983; 65(2):134-8. PubMed ID: 6654327
[TBL] [Abstract][Full Text] [Related]
9. Chromosome 6q- and associated malformations.
Liberfarb RM; Atkins L; Holmes LB
Ann Genet; 1978 Dec; 21(4):223-5. PubMed ID: 314259
[TBL] [Abstract][Full Text] [Related]
10. Interstitial deletion of band q12 of chromosome 5.
Dudin G; Alexander D; Talj F; Deeb M; Musallam S; Der Kaloustian VM
Clin Genet; 1984 May; 25(5):455-8. PubMed ID: 6723107
[TBL] [Abstract][Full Text] [Related]
11. A girl with an interstitial deletion of the short arm of chromosome 3 studied with a high-resolution banding technique.
Sichong Z; Bui TH; Castro I; Iselius L; Håkansson S; Lundmark KM
Hum Genet; 1981; 59(2):178-81. PubMed ID: 7327578
[TBL] [Abstract][Full Text] [Related]
12. Partial deletion of the short arm of chromosome 12(p11; p13). Report of a case.
Tenconi R; Baccichetti C; Anglani F; Pellergrino PA; Kaplan JC; Junien C
Ann Genet; 1975 Jun; 18(2):95-8. PubMed ID: 1081371
[TBL] [Abstract][Full Text] [Related]
13. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
Taysi K; Sekhon GS; Hillman RE
Am J Med Genet; 1982 Dec; 13(4):423-30. PubMed ID: 7158642
[No Abstract] [Full Text] [Related]
14. Interstitial deletion of the long arm of chromosome 2: a clinically recognizable microdeletion syndrome?
Maas SM; Hoovers JM; van Seggelen ME; Menzel DM; Hennekam RC
Clin Dysmorphol; 2000 Jan; 9(1):47-53. PubMed ID: 10649798
[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. Interstitial deletion of the long arm of chromosome 6 [del(6) (q16q22)]: case report and review of the literature.
Schwartz MF; Kaffe S; Wallace S; Desnick RJ
Clin Genet; 1984 Dec; 26(6):574-8. PubMed ID: 6499269
[TBL] [Abstract][Full Text] [Related]
17. Deletion 1q42.3----qter in a girl with psychomotoric retardation and multiple dysmorphisms.
Kausch K; Köhler J; Schmid M
Ann Genet; 1988; 31(3):193-4. PubMed ID: 3265611
[TBL] [Abstract][Full Text] [Related]
18. Two cases of the Langer-Giedion syndrome with the same interstitial deletion of the long arm of chromosome 8: 46, XY or XX, del (8) (q23.3q24.13).
Fukushima Y; Kuroki Y; Izawa T
Hum Genet; 1983; 64(1):90-3. PubMed ID: 6336324
[TBL] [Abstract][Full Text] [Related]
19. The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction.
Bergamo F; Crosato F; Francesconi D; Pasqual F; Zuffardi O
Clin Genet; 1977 Mar; 11(3):219-23. PubMed ID: 837573
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
