247 related articles for article (PubMed ID: 7294066)
1. Meiotic consequences of pericentric inversions of chromosome 13.
Wenger SL; Steele MW
Am J Med Genet; 1981; 9(4):275-83. PubMed ID: 7294066
[TBL] [Abstract][Full Text] [Related]
2. Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 leads to 14qter).
Trunca C; Opitz JM
Am J Med Genet; 1977; 1(2):217-28. PubMed ID: 610431
[TBL] [Abstract][Full Text] [Related]
3. [Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].
Scarinci R; Anichini C; Vivarelli R; Berardi R; Pucci L; Rosaia L; Tomaccini D
Boll Soc Ital Biol Sper; 1992 Mar; 68(3):175-81. PubMed ID: 1389073
[TBL] [Abstract][Full Text] [Related]
4. Inherited parital duplication deficiency of chromosome 15 (p12;q22).
Coco R; Penchaszadeh VB
J Genet Hum; 1978 Sep; 26(3):203-10. PubMed ID: 739260
[TBL] [Abstract][Full Text] [Related]
5. Familial paracentric inversion of the short arm of chromosome 3.
Fryns JP; van den Berghe H
Ann Genet; 1979; 22(3):163-4. PubMed ID: 316673
[TBL] [Abstract][Full Text] [Related]
6. Pericentric inversions of the X chromosome. A new observation and review of the published cases.
Pfeiffer RA; Kossakiewicz M; Baisch C
J Genet Hum; 1986 Aug; 34(3-4):331-7. PubMed ID: 3760837
[TBL] [Abstract][Full Text] [Related]
7. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22).
Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM
Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399
[TBL] [Abstract][Full Text] [Related]
8. [Severe mental retardation and slight dysmorphism in a child with a bisatellite extrachromosome: inversion duplication (15)?].
Rinaldi MM; Militerni R; Pascotto A; Scarano G; Renda S; Cavaliere ML; Santulli B; Esposito M; Ventruto V
Pediatr Med Chir; 1982; 4(5):559-61. PubMed ID: 6927358
[TBL] [Abstract][Full Text] [Related]
9. Supernumerary small chromosomal anomaly: report of three cases including one with a familial inversion of chromosome 5.
Lee Ml; Schneider J; Wasant P; Yu CY; Trpis L; Liang YW; Lewis BM; Borkowf S; Borgaonkar DS
J Genet Hum; 1978 Sep; 26(3):275-85. PubMed ID: 739263
[TBL] [Abstract][Full Text] [Related]
10. [Pericentric inversion of chromosome 9. Summary of the authors' results].
Vargas de los Monteros MT; Fernández-Novoa García MC; Salas Herrero E; San Martín Díez MV; Novales Huertas MA
An Esp Pediatr; 1990 Nov; 33(5):442-9. PubMed ID: 2096758
[TBL] [Abstract][Full Text] [Related]
11. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
12. Familial 10p trisomy resulting from a maternal pericentric inversion.
Kozma C; Meck JM
Am J Med Genet; 1994 Feb; 49(3):281-7. PubMed ID: 8209887
[TBL] [Abstract][Full Text] [Related]
13. Frequency and association of NOR's in a family carrying a pericentric inversion of chromosome 14.
Leal-Garza C; Riojas-Valdés V; Montes de Oca-Luna R; Garza-Chapa R
Rev Invest Clin; 1984; 36(3):283-6. PubMed ID: 6542690
[No Abstract] [Full Text] [Related]
14. De novo 13q paracentric inversion in a boy with cleft palate and mental retardation.
Riccardi VM; Holmquist GP
Hum Genet; 1979 Nov; 52(2):211-5. PubMed ID: 511176
[TBL] [Abstract][Full Text] [Related]
15. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
16. Six cases of partial duplication-deficiency 21 syndrome: 21(dupq22delp23) due to maternal pericentric inversion: inv(21)(p12;q22). A family study.
Fraisse J; Philip T; Bertheas MF; Lauras B
Ann Genet; 1986; 29(3):177-80. PubMed ID: 2947533
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic study of a family with an aberrant inv ((15p+ q-) chromosome inherited through five generations.
Podugol'nikova OA; Batienko GS
Sov Genet; 1974 May; 8(4):518-25. PubMed ID: 4412695
[No Abstract] [Full Text] [Related]
18. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
[TBL] [Abstract][Full Text] [Related]
19. [Pericentric inversion of human chromosomes and its risks] ].
Balícek P
Cas Lek Cesk; 2001 Feb; 140(2):38-42. PubMed ID: 11262905
[TBL] [Abstract][Full Text] [Related]
20. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]