88 related articles for article (PubMed ID: 3981143)
1. Familial inv(2) (p2300q11.2).
Sole-Pujol MT; Rivera H; Castro-Felix LP; Moller M; Cantu JM
J Genet Hum; 1985 Jan; 33(1):57-62. PubMed ID: 3981143
[TBL] [Abstract][Full Text] [Related]
2. inv(5)(p13q13) in a four generation pedigree.
Vargas-Moyeda E; Rivera H; Garcia-Cruz D; Moller M; Cantu JM
J Genet Hum; 1987 Aug; 35(4):305-8. PubMed ID: 3655755
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Familial pericentric inversion of the X chromosome [inv(X)(p11q28)]].
Baumann W; Zabel B; Holl M
Ann Genet; 1984; 27(2):106-8. PubMed ID: 6331785
[TBL] [Abstract][Full Text] [Related]
5. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
Butomo IV; Prozorova MV; Khitrikova LE
Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
[TBL] [Abstract][Full Text] [Related]
6. Familial pericentric inversion of chromosome 13, 46,XX,inv (13)(p13;q11): a new variant.
Mohammed FM; Krishna Murthy DS; Farag TI; al-Awadi SA; al-Othman SA; Hammad I
Ann Genet; 1993; 36(3):181-5. PubMed ID: 8117067
[TBL] [Abstract][Full Text] [Related]
7. Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.
Stine SB; Clark CE; Telfer MA; Casey PA; Cowell HR
Am J Med Genet; 1982 May; 12(1):57-62. PubMed ID: 7091197
[TBL] [Abstract][Full Text] [Related]
8. Familial paracentric inversion inv(2)(q31q36).
Schmid M; Hofmann R; Köhler J; Jannek U
Hum Genet; 1985; 71(3):270-2. PubMed ID: 4065899
[TBL] [Abstract][Full Text] [Related]
9. [Paracentric inversions in man. Apropos of 2 familial observations].
Morichon-Delvallez N; Marchand F
Ann Genet; 1985; 28(2):119-22. PubMed ID: 3876061
[TBL] [Abstract][Full Text] [Related]
10. Familial robertsonian translocation 15;21 and rare paracentric inv(21): unexpected re-inversion in a child with translocation trisomy 21.
Mau UA; Petruch UR; Kaiser P; Eggermann T
Eur J Hum Genet; 2000 Nov; 8(11):815-9. PubMed ID: 11093270
[TBL] [Abstract][Full Text] [Related]
11. Familial pericentric inversion (10) and its effect on two offspring.
Rodriguez MT; Martin MJ; Abrisqueta JA
J Med Genet; 1984 Aug; 21(4):317-9. PubMed ID: 6492099
[TBL] [Abstract][Full Text] [Related]
12. Mosaic inversion duplication of chromosome 15 without phenotypic effect: occurrence in a father and daughter.
Knight LA; Lipson M; Mann J; Bachman R
Am J Med Genet; 1984 Mar; 17(3):649-54. PubMed ID: 6585144
[TBL] [Abstract][Full Text] [Related]
13. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
[TBL] [Abstract][Full Text] [Related]
14. Reproductive failure in a carrier of inv dupl l(q21.4----q12).
Toncheva D; Genkova P; Tzoneva M; Lozanova T; Angelova E; Mitreva B
Acta Paediatr Hung; 1986; 27(1):61-6. PubMed ID: 3730184
[TBL] [Abstract][Full Text] [Related]
15. Familial paracentric inversion inv(3)(q21q25.1). Case report and review of the literature.
Djalali M; Steinbach P; Barbi G
Ann Genet; 1984; 27(1):41-4. PubMed ID: 6372643
[TBL] [Abstract][Full Text] [Related]
16. Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literature.
Hales HA; Peterson CM; Carey J; Hecht BK; Hecht F
Am J Med Genet; 1993 Nov; 47(6):848-51. PubMed ID: 8279482
[TBL] [Abstract][Full Text] [Related]
17. Familial pericentric inversion of chromosome 2.
Mattevi MS; Pinheiro CE; Erdtmann B; Flores RZ; Salzano FM
J Genet Hum; 1981 Jun; 29(2):161-9. PubMed ID: 7328411
[TBL] [Abstract][Full Text] [Related]
18. A small one-band paracentric inversion inv (4) (p15.3p16.3).
Smith A; Watt AJ; Cummins M; Gardner RJ; Wilson M
Ann Genet; 1992; 35(3):161-3. PubMed ID: 1466565
[TBL] [Abstract][Full Text] [Related]
19. Familial inv(1) (p3500q21.3) associated with azoospermia.
Rivera H; Alvarez-Arratia MC; Moller M; Díaz M; Cantú JM
Hum Genet; 1984; 66(2-3):165-7. PubMed ID: 6714976
[TBL] [Abstract][Full Text] [Related]
20. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
Spinner NB; Zackai E; Cheng SD; Knoll JH
Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]