103 related articles for article (PubMed ID: 1605251)
1. 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]
2. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Interstitial tandem direct duplication of the long arm of chromosome 4 (q23-q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segment.
Halal F; Vekemans M; Chitayat D
Am J Med Genet; 1991 Jun; 39(4):418-21. PubMed ID: 1877620
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
[TBL] [Abstract][Full Text] [Related]
11. Decreased cell viability of fibroblasts from two patients with a ring chromosome: an in vitro reflection of growth failure?
Kosztolányi G
Am J Med Genet; 1987 Sep; 28(1):181-4. PubMed ID: 3674110
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
Cappon SL; Duncan AM; Khalifa MM
Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
[TBL] [Abstract][Full Text] [Related]
14. Ring chromosome 22 resulting in partial monosomy in a mentally retarded boy.
Gibbons B; Tan SY; Tam PY
Singapore Med J; 1999 Apr; 40(4):273-5. PubMed ID: 10487083
[TBL] [Abstract][Full Text] [Related]
15. Ring chromosome 6: report of a patient and literature review.
Chitayat D; Hahm SY; Iqbal MA; Nitowsky HM
Am J Med Genet; 1987 Jan; 26(1):145-51. PubMed ID: 3544845
[TBL] [Abstract][Full Text] [Related]
16. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
19. Ring chromosome 22 and autism: report and review.
MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
[TBL] [Abstract][Full Text] [Related]
20. A boy with ring chromosome 15 derived from a t(15q;15q) Robertsonian translocation in the mother: cytogenetic and biochemical findings.
Neri G; Ricci R; Pelino A; Bova R; Tedeschi B; Serra A
Am J Med Genet; 1983 Feb; 14(2):307-14. PubMed ID: 6220608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
