141 related articles for article (PubMed ID: 6974530)
1. Ring chromosome 11 [46,XX,r(11) (p15q25)] associated with clinical features of the 11q- syndrome.
Niikawa N; Jinno Y; Tomiyasu T; Fukushima Y; Kudo K
Ann Genet; 1981; 24(3):172-5. PubMed ID: 6974530
[TBL] [Abstract][Full Text] [Related]
2. A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletion.
Morava E; Bartsch O; Czako M; Frensel A; Kárteszi J; Kosztolányi GY
Genet Couns; 2003; 14(3):337-42. PubMed ID: 14577679
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Chromosome 11 long arm partial deletion: a new syndrome.
Engel E; Hirshberg CS; Cassidy SB; McGee BJ
Am J Ment Defic; 1976 Jan; 80(4):473-5. PubMed ID: 1247044
[TBL] [Abstract][Full Text] [Related]
5. The syndrome of ring chromosome 12.
Scribanu N; McCullars EB; Baumiller RC; Colon AR
Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
[TBL] [Abstract][Full Text] [Related]
6. Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q.
Cousineau AJ; Higgins JV; Scott-Emuakpor AB; Mody G
Am J Med Genet; 1983 Jan; 14(1):29-35. PubMed ID: 6829609
[TBL] [Abstract][Full Text] [Related]
7. 11q- syndrome: three cases and a review of the literature.
Leegte B; Kerstjens-Frederikse WS; Deelstra K; Begeer JH; van Essen AJ
Genet Couns; 1999; 10(3):305-13. PubMed ID: 10546104
[TBL] [Abstract][Full Text] [Related]
8. Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome.
Tamura T; Tohma T; Ohta T; Soejima H; Harada N; Abe K; Niikawa N
Clin Dysmorphol; 1993 Apr; 2(2):106-13. PubMed ID: 7506614
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 10q in three unrelated patients.
Taysi K; Yang V; Monaghan N; Beraha N
Ann Genet; 1983; 26(2):79-85. PubMed ID: 6604490
[TBL] [Abstract][Full Text] [Related]
10. A clinical syndrome associated with 5p duplication and 9p deletion.
Liberfarb RM; Atkins L; Holmes LB
Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
[TBL] [Abstract][Full Text] [Related]
11. Partial monosomy of the long arm of chromosome 11 in a severely affected child.
Lee ML; Sciorra LJ
Ann Genet; 1981; 24(1):51-3. PubMed ID: 6971620
[TBL] [Abstract][Full Text] [Related]
12. Partial 8p- syndrome.
Patil SR; Hanson JW
J Genet Hum; 1980 Dec; 28(4):123-9. PubMed ID: 7205196
[TBL] [Abstract][Full Text] [Related]
13. Terminal deletion of the short arm of chromosome 3, del(3pter-p25): a recognizable syndrome.
Schwyzer U; Binkert F; Caflisch U; Baumgartner B; Schinzel A
Helv Paediatr Acta; 1987; 42(4):309-15. PubMed ID: 3443553
[TBL] [Abstract][Full Text] [Related]
14. [Ring chromosome 13 and multiple malformations (author's transl)].
Antich J; Plaza J; Geán E
An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
[TBL] [Abstract][Full Text] [Related]
15. Two cases of ring chromosome 13. Chromosome banding patterns and mosaic configuration.
Steinbach P; Drews K; Horstmann W; Barbi G; Scholz W
Ann Genet; 1981; 24(3):152-7. PubMed ID: 6974524
[TBL] [Abstract][Full Text] [Related]
16. Partial monosomy for a 21 chromosome. Report of a new case of r(21) and review of the literature.
Ferrante E; Vignetti P; Antonelli M; Bruni L; Bertasi S; Chessa L
Helv Paediatr Acta; 1983 Mar; 38(1):73-80. PubMed ID: 6345474
[TBL] [Abstract][Full Text] [Related]
17. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
18. Phenotype associated with ring 10 chromosome: report of patient and review of literature.
Michels VV; Driscoll DJ; Ledbetter DH; Riccardi VM
Am J Med Genet; 1981; 9(3):231-7. PubMed ID: 7025632
[TBL] [Abstract][Full Text] [Related]
19. Partial monosomy 11q and trisomy 12q: variable expression in two siblings.
Lukusa T; Holvoet M; Vermeesch JR; Devriendt K; Fryns JP
Genet Couns; 2003; 14(2):155-64. PubMed ID: 12872809
[TBL] [Abstract][Full Text] [Related]
20. Emerging phenotype of duplication (7p): a report of three cases and review of the literature.
Milunsky JM; Wyandt HE; Milunsky A
Am J Med Genet; 1989 Jul; 33(3):364-8. PubMed ID: 2679090
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]