149 related articles for article (PubMed ID: 6331787)
1. Mild expression of 3qter trisomy due to a de novo (X;3)(p22.3;q25.3) translocation.
Rivera H; Möller M; Arreola R; Cantu JM
Ann Genet; 1984; 27(2):112-4. PubMed ID: 6331787
[TBL] [Abstract][Full Text] [Related]
2. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
[TBL] [Abstract][Full Text] [Related]
3. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
[TBL] [Abstract][Full Text] [Related]
4. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
Canún S; Mutchinick O; Shaffer LG; Fernández C
Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
[TBL] [Abstract][Full Text] [Related]
6. X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivation.
Preis W; Barbi G; Liptay S; Kennerknecht I; Schwemmle S; Pohlandt F
Am J Med Genet; 1996 Jan; 61(2):117-21. PubMed ID: 8669435
[TBL] [Abstract][Full Text] [Related]
7. [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
Morichon-Delvallez N; Couturier J; Frison B
Ann Genet; 1982; 25(4):246-8. PubMed ID: 6985016
[TBL] [Abstract][Full Text] [Related]
8. Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: prenatal and postnatal late replication studies.
Zori RT; Gray BA; Bent-Williams A; Driscoll DJ; Williams CA; Zackowski JL
Am J Med Genet; 1993 Jun; 46(4):379-83. PubMed ID: 8357008
[TBL] [Abstract][Full Text] [Related]
9. Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation.
Zuffardi O; Tiepolo L; Scappaticci S; Francesconi D; Bianchi C; di Natale D
Ann Genet; 1977 Sep; 20(3):191-94. PubMed ID: 304704
[TBL] [Abstract][Full Text] [Related]
10. Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23.
Kulharya AS; Roop H; Kukolich MK; Nachtman RG; Belmont JW; Garcia-Heras J
Am J Med Genet; 1995 Mar; 56(1):16-21. PubMed ID: 7747779
[TBL] [Abstract][Full Text] [Related]
11. [Unbalanced translocation 8/X in a girl].
Ickstadt A; Palitzsch D; Foerster W; Fuhrmann-Rieger A
Monatsschr Kinderheilkd; 1989 Apr; 137(4):239-42. PubMed ID: 2733701
[TBL] [Abstract][Full Text] [Related]
12. Spreading of inactivation in an (X;14) translocation.
Allderdice PW; Miller OJ; Miller DA; Klinger HP
Am J Med Genet; 1978; 2(3):233-40. PubMed ID: 263441
[TBL] [Abstract][Full Text] [Related]
13. Azoospermia and duplication 3qter as distinct consequences of a familial t(X;3) (q26;q13.2).
Cantú JM; Díaz M; Möller M; Jiménez-Sáinz M; Sandoval L; Vaca G; Rivera H
Am J Med Genet; 1985 Apr; 20(4):677-84. PubMed ID: 3993688
[TBL] [Abstract][Full Text] [Related]
14. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
Siffroi JP; Romani F; Viguié F; Lejeune C
Ann Genet; 1984; 27(4):241-4. PubMed ID: 6335372
[TBL] [Abstract][Full Text] [Related]
15. Mild phenotype and normal gonadal function in females with 4p trisomy due to unbalanced t(X;4)(p22.1;p14).
Petit P; Hilliker C; Van Leuven F; Fryns JP
Clin Genet; 1994 Oct; 46(4):304-8. PubMed ID: 7834896
[TBL] [Abstract][Full Text] [Related]
16. DNA replication sequence in a dicentric (functionally monocentric) X chromosome formed by the joining of two X chromosomes at region p22.
Yu CW; Priest JH; Byrd JR
Am J Med Genet; 1982 Mar; 11(3):305-17. PubMed ID: 7081296
[TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 3q due to a de novo translocation t(X;3) (p21;q12).
Oorthuys JW; Slater RM; Barrowclough H; de Kleine MJ
Clin Genet; 1981 Aug; 20(2):130-4. PubMed ID: 7307309
[TBL] [Abstract][Full Text] [Related]
18. Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23).
Solé MT; Rivera H; Sánchez-Corona J; Plascencia L; Cantú JM
Ann Genet; 1983; 26(2):120-2. PubMed ID: 6604487
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21.
Cardoso LC; Moraes L; Camilo MJ; Mulatinho MV; Ramos H; Almeida JC; Llerena JC; Seuánez HN; Vargas FR
Eur J Med Genet; 2008; 51(6):588-97. PubMed ID: 18674646
[TBL] [Abstract][Full Text] [Related]
20. Rescue from the effects of trisomy 13q32-->qter owing to skewed X inactivation in a der(X)t(X;13)(p21;q32) carrier.
Blennow E; Sahlén S
J Med Genet; 1999 Sep; 36(9):718-9. PubMed ID: 10507733
[No Abstract] [Full Text] [Related]
[Next] [New Search]
