91 related articles for article (PubMed ID: 6170224)
1. Ring 14 chromosome: association with seizures.
Lippe BM; Sparkes RS
Am J Med Genet; 1981; 9(4):301-5. PubMed ID: 6170224
[TBL] [Abstract][Full Text] [Related]
2. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.
Melnyk AR; Dewald G
Am J Med Genet; 1994 Mar; 50(1):12-4. PubMed ID: 7512788
[TBL] [Abstract][Full Text] [Related]
3. Deletion (9) (p13.1 p21.1).
Scaglia F; Bodamer OA; Berend SA; Adam LR; Shaffer LG
Am J Med Genet; 2000 Mar; 91(2):113-5. PubMed ID: 10748408
[TBL] [Abstract][Full Text] [Related]
4. Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.
Chodirker BN; Ray M; McAlpine PJ; Riordan D; Vust A; Pugh D; Chudley AE
Am J Med Genet; 1988 Sep; 31(1):145-51. PubMed ID: 2464927
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
[TBL] [Abstract][Full Text] [Related]
7. Autism and hypoplastic corpus callosum in a case of monocentric marker chromosome 15.
Jovanović-Privrodski JD; Kavecan II; Obrenović MR; Buonadonna LA; Bukvić NM
Pediatr Neurol; 2009 Jul; 41(1):65-7. PubMed ID: 19520280
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
Fang YY; Bain S; Haan EA; Eyre HJ; MacDonald M; Wright TJ; Altherr MR; Riess O; Sutherland G; Callen DF
Am J Med Genet; 1997 Sep; 71(4):453-7. PubMed ID: 9286454
[TBL] [Abstract][Full Text] [Related]
10. Dir dup(X) (q13-->qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomalies.
Aughton DJ; AlSaadi AA; Johnson JA; Transue DJ; Trock GL
Am J Med Genet; 1993 Apr; 46(2):159-64. PubMed ID: 7683452
[TBL] [Abstract][Full Text] [Related]
11. A ring 14 chromosome with deleted short arm.
Amarose AP; Dorus E; Huttenlocher PR; Csaszar S
Hum Genet; 1980; 54(2):145-7. PubMed ID: 6156115
[TBL] [Abstract][Full Text] [Related]
12. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
Bibas Bonet H; Fontenla M; Fauze R; G de Pinat I
Rev Neurol; 2001 Apr 16-30; 32(8):746-50. PubMed ID: 11391511
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
[TBL] [Abstract][Full Text] [Related]
14. Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.
Popp S; Schulze B; Granzow M; Keller M; Holtgreve-Grez H; Schoell B; Brough M; Hager HD; Tariverdian G; Brown J; Kearney L; Jauch A
Hum Genet; 2002 Jul; 111(1):31-9. PubMed ID: 12136233
[TBL] [Abstract][Full Text] [Related]
15. Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.
Schrander-Stumpel CT; Govaerts LC; Engelen JJ; van der Blij-Philipsen M; Borghgraef M; Loots WJ; Peters JJ; Rijnvos WP; Smeets DF; Fryns JP
Am J Med Genet; 1994 May; 50(4):377-80. PubMed ID: 7516121
[TBL] [Abstract][Full Text] [Related]
16. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
[TBL] [Abstract][Full Text] [Related]
17. [Ring-20 chromosome: a new syndrome].
Jalbert P; Jalbert H; Sele B; Tachker D; Bost M; Meynard R; Pison H
Ann Genet; 1977 Dec; 20(4):258-62. PubMed ID: 305753
[TBL] [Abstract][Full Text] [Related]
18. Supernumerary chromosome marker (1) in a developmentally delayed child.
Lanphear N; Lamb A; Oppenheimer S; Soukup S
Am J Med Genet; 1995 Jul; 57(3):400-2. PubMed ID: 7545867
[TBL] [Abstract][Full Text] [Related]
19. Terminal deletion of long arm of chromosome 4: patient report and literature review.
Evers LJ; Schrander-Stumpel CT; Engelen JJ; Mulder H; Borghgraef M; Fryns JP
Genet Couns; 1993; 4(2):139-45. PubMed ID: 7689326
[TBL] [Abstract][Full Text] [Related]
20. Further delineation of the chromosome 14q terminal deletion syndrome.
van Karnebeek CD; Quik S; Sluijter S; Hulsbeek MM; Hoovers JM; Hennekam RC
Am J Med Genet; 2002 Jun; 110(1):65-72. PubMed ID: 12116274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]