279 related articles for article (PubMed ID: 511176)
1. 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]
2. High resolution pattern of an inverted duplication (15).
Hoo JJ
Clin Genet; 1986 Mar; 29(3):241-5. PubMed ID: 3457663
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.
Sparkes RS; Muller H; Klisak I
Science; 1979 Mar; 203(4384):1027-9. PubMed ID: 424728
[TBL] [Abstract][Full Text] [Related]
5. Familial pericentric inversion inv(8)(p23q11).
Boyd H; Kaste J; Hovi E; Ritanen-Mohammed UM; Kääriäinen H; de la Chapelle A; Lehesjoki AE
J Med Genet; 1994 Mar; 31(3):201-5. PubMed ID: 8014967
[TBL] [Abstract][Full Text] [Related]
6. Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.
Sloan-Béna F; Philippe C; LeHeup B; Wuilque F; Levy ER; Chéry M; Jonveaux P; Monaco AP
J Med Genet; 1998 Feb; 35(2):146-50. PubMed ID: 9507395
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).
Jaeken J; Fryns JP; Standaert L; De Cock P; Van den Berghe H
Ann Genet; 1980; 23(2):105-7. PubMed ID: 6967281
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
Sanchez O; Yunis JJ; Escobar JI
Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
[No Abstract] [Full Text] [Related]
10. Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardation.
Schwanitz G; Schmid P; Hägele C; Daffner HW; Grosse KP
Acta Genet Med Gemellol (Roma); 1977; 26(2):173-5. PubMed ID: 596113
[TBL] [Abstract][Full Text] [Related]
11. Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.
Phelan MC; Stevenson RE; Anderson EV
Am J Med Genet; 1993 May; 46(3):304-8. PubMed ID: 8488876
[TBL] [Abstract][Full Text] [Related]
12. A, 1;6, translocation associated with congenital glaucoma and cleft lip and palate.
Tinning S; Jacobsen P; Mikkelsen M
Hum Hered; 1975; 25(6):453-60. PubMed ID: 1225819
[TBL] [Abstract][Full Text] [Related]
13. Fragile site at 12q13 associated with phenotypic abnormalities.
Morić-Petrović S; Laca Z
J Med Genet; 1984 Jun; 21(3):216-7. PubMed ID: 6748019
[TBL] [Abstract][Full Text] [Related]
14. Analysis of banding patterns in a case of ring chromosome 21.
Richer CL; Fitch N; Sitahal S; Murer-Orlando M; Jean P
Am J Med Genet; 1981; 10(4):323-31. PubMed ID: 7332027
[No Abstract] [Full Text] [Related]
15. 13S+. Giant satellites or de novo rearrangement?
Imaizumi K; Kajii T; Niikawa N
Hum Genet; 1981; 59(3):266-8. PubMed ID: 7327588
[TBL] [Abstract][Full Text] [Related]
16. Familial paracentric inversion of 1p.
Romain DR; Columbano-Green LM; Whyte S; Smythe RH; Parfitt RG; Gebbie OB; Chapman CJ
Am J Med Genet; 1983 Apr; 14(4):629-34. PubMed ID: 6846398
[TBL] [Abstract][Full Text] [Related]
17. A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardation.
Neetha J; Girisha KM; Gopinath PM; Sekhar MR
Genet Couns; 2012; 23(4):473-6. PubMed ID: 23431746
[TBL] [Abstract][Full Text] [Related]
18. Cytogenetic characterization of an extra structurally abnormal chromosome associated with severe mental retardation: inv dup (15) (q13).
Gorla N; Slavutsky I; Lisanti J; Pedrazzini E; Vanella L; Larripa I
Hereditas; 1998; 129(1):1-5. PubMed ID: 9868924
[TBL] [Abstract][Full Text] [Related]
19. Supernumerary small ring chromosome.
Kaffe S; Kim HJ; Hsu LY; Brill CB; Hirschhorn K
J Med Genet; 1977 Dec; 14(6):447-51. PubMed ID: 604496
[TBL] [Abstract][Full Text] [Related]
20. Familial 13p+ chromosome with mental retardation and dysmorphic features of two children.
Stoll C; Rohmer A; Korn R; Heumann G
Hum Genet; 1976 Sep; 34(1):81-4. PubMed ID: 965011
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
