138 related articles for article (PubMed ID: 3189413)
1. Ring chromosome 11 and café-au-lait spots.
Fagan K; Suthers GK; Hardacre G
Am J Med Genet; 1988 Aug; 30(4):911-6. PubMed ID: 3189413
[TBL] [Abstract][Full Text] [Related]
2. Ring chromosome 12.
Park JP; Graham JM; Andrews PA; Wurster-Hill DH
Am J Med Genet; 1988 Feb; 29(2):437-40. PubMed ID: 3354616
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Ring chromosome 18 in a mother and son.
Donlan MA; Dolan CR
Am J Med Genet; 1986 May; 24(1):171-4. PubMed ID: 3706404
[TBL] [Abstract][Full Text] [Related]
5. Case of ring chromosome 7: the first report of neuropathological findings.
Tsukamoto H; Sakai N; Taniike M; Nakatsukasa M; Yoshiwara W; Sakamoto H; Fujimura H; Inui K; Okada S
Am J Med Genet; 1993 Jul; 46(6):632-5. PubMed ID: 8362903
[TBL] [Abstract][Full Text] [Related]
6. Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots.
Brunner HG; Hulsebos T; Steijlen PM; der Kinderen DJ; vd Steen A; Hamel BC
Am J Med Genet; 1993 Jun; 46(4):472-4. PubMed ID: 8357027
[TBL] [Abstract][Full Text] [Related]
7. Ring chromosome 17 in a mentally retarded boy.
Qazi OH; Madahar C; Kanchanapoomi R; Giridharan R; Beller E
Ann Genet; 1979; 22(4):234-8. PubMed ID: 121681
[TBL] [Abstract][Full Text] [Related]
8. Autosomal dominant multiple café-au-lait spots and neurofibromatosis-1: evidence of non-linkage.
Charrow J; Listernick R; Ward K
Am J Med Genet; 1993 Mar; 45(5):606-8. PubMed ID: 8456833
[TBL] [Abstract][Full Text] [Related]
9. Johnson-McMillin syndrome: report of another family.
Hennekam RC; Holtus FJ
Am J Med Genet; 1993 Oct; 47(5):714-6. PubMed ID: 8267002
[TBL] [Abstract][Full Text] [Related]
10. Two patients with ring chromosome 15 syndrome.
Butler MG; Fogo AB; Fuchs DA; Collins FS; Dev VG; Phillips JA
Am J Med Genet; 1988 Jan; 29(1):149-54. PubMed ID: 3278612
[TBL] [Abstract][Full Text] [Related]
11. Ring chromosome 7: report of the fifth case.
Caramia GM; Baroncini A; Osimani P; Forabosco A
Eur J Pediatr; 1990 Apr; 149(7):475-6. PubMed ID: 2189730
[TBL] [Abstract][Full Text] [Related]
12. Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase-L to the distal segment of the long arm of chromosome 20.
Halal F; Chitayat D; Parikh H; Rosenblatt B; Tranchemontagne J; Vekemans M; Potier M
Am J Med Genet; 1992 Jun; 43(3):576-9. PubMed ID: 1605251
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Leiomyoma of uterus in a patient with ring chromosome 12: case presentation and literature review.
Hajianpour MJ; Hajianpour AK; Habibian R; Wohlmuth C
Am J Med Genet; 1996 May; 63(2):335-9. PubMed ID: 8725781
[TBL] [Abstract][Full Text] [Related]
15. Flecked retina associated with café au lait spots, microcephaly, epilepsy, short stature, and ring 17 chromosome.
Gass JD; Taney BS
Arch Ophthalmol; 1994 Jun; 112(6):738-9. PubMed ID: 8002828
[No Abstract] [Full Text] [Related]
16. Ring chromosome 15 syndrome. Further delineation of the adult phenotype.
Fryns JP; Kleczkowska A; Buttiens M; Jonckheere P; Brouckmans-Buttiens K; van den Berghe H
Ann Genet; 1986; 29(1):45-8. PubMed ID: 3487276
[No Abstract] [Full Text] [Related]
17. Stable ring chromosome 21: molecular and clinical definition of the lesion.
Falik-Borenstein TC; Pribyl TM; Pulst SM; Van Dyke DL; Weiss L; Chu ML; Kraus J; Marshak D; Korenberg JR
Am J Med Genet; 1992 Jan; 42(1):22-8. PubMed ID: 1308361
[TBL] [Abstract][Full Text] [Related]
18. Cafe au lait has hue of its own.
Orion E; Matz H; Wolf D; Wolf R
Dermatol Online J; 2003 Dec; 9(5):8. PubMed ID: 14996381
[TBL] [Abstract][Full Text] [Related]
19. Ring chromosome 6: clinical and cytogenetic behaviour.
Paz-y-Miño C; Benítez J; Ayuso C; Sánchez-Cascos A
Am J Med Genet; 1990 Apr; 35(4):481-3. PubMed ID: 2333874
[TBL] [Abstract][Full Text] [Related]
20. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
Migliori MV; Cherubini V; Bartolotta E; Pettinari A; Pecora R
Am J Med Genet; 1994 Jan; 49(1):108-10. PubMed ID: 8172236
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
