209 related articles for article (PubMed ID: 8423613)
1. Reproductive possibilities for balanced translocation (14) carriers in families with partial trisomy of proximal 14q.
Valkova G; Stefanova M
J Med Genet; 1993 Jan; 30(1):73-5. PubMed ID: 8423613
[TBL] [Abstract][Full Text] [Related]
2. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.
Voss R; Gross-Kieselstein E; Hurvitz H; Dagan J; Kerem E; Zlotogora J
J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835
[TBL] [Abstract][Full Text] [Related]
3. [Partial trisomy 14q II.--Partial trisomy 14q due to a maternal t(12; 14) (q24.4; q21)].
Turleau C; Grouchy J; Bocquentin F; Roubin M; Colin FC
Ann Genet; 1975 Mar; 18(1):41-4. PubMed ID: 1080037
[TBL] [Abstract][Full Text] [Related]
4. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
5. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].
Grasshoff U; Singer S; Liehr T; Starke H; Fode B; Schöning M; Dufke A
Cytogenet Genome Res; 2003; 103(1-2):17-23. PubMed ID: 15004458
[TBL] [Abstract][Full Text] [Related]
6. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
Frankova YE; Holenova H; Braulke I
Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
[TBL] [Abstract][Full Text] [Related]
7. Trisomy 6q25 leads to 6qter in two sisters resulting from maternal 6;11 translocation.
Clark CE; Cowell HR; Telfer MA; Casey PA
Am J Med Genet; 1980; 5(2):171-8. PubMed ID: 7395910
[TBL] [Abstract][Full Text] [Related]
8. [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)].
Raoul O; Rethoré MO; Dutriliaux B; Michon L; Lejeune J
Ann Genet; 1975 Mar; 18(1):35-9. PubMed ID: 1080036
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.
Simpson J; Zellweger H
J Med Genet; 1977 Apr; 14(2):124-7. PubMed ID: 853318
[TBL] [Abstract][Full Text] [Related]
10. A familial "balanced" 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings.
Wagstaff J; Hemann M
Am J Hum Genet; 1995 Jan; 56(1):302-9. PubMed ID: 7825591
[TBL] [Abstract][Full Text] [Related]
11. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
Cohen MM; Ornoy A; Rosenmann A; Kohn G
Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
[TBL] [Abstract][Full Text] [Related]
12. Partial trisomy 7p associated with familial 7p;22q translocation.
Larson LM; Wasdahl WA; Jalal SM
J Med Genet; 1977 Aug; 14(4):258-61. PubMed ID: 926137
[TBL] [Abstract][Full Text] [Related]
13. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.
Smeets D; van Ravenswaaij C; de Pater J; Gerssen-Schoorl K; Van Hemel J; Janssen G; Smits A
J Med Genet; 1997 Jan; 34(1):18-23. PubMed ID: 9032644
[TBL] [Abstract][Full Text] [Related]
14. A case of severe mental and developmental retardation associated with 14q terminal monosomy/5q terminal trisomy.
Hirayama T
J Nippon Med Sch; 2010 Feb; 77(1):40-4. PubMed ID: 20154457
[TBL] [Abstract][Full Text] [Related]
15. Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.
Stengel-Rutkowski S; Lohse K; Herzog C; Apacik C; Couturier J; Albert A; Belohradsky B
Clin Genet; 1992 Oct; 42(4):178-85. PubMed ID: 1424241
[TBL] [Abstract][Full Text] [Related]
16. Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.
Walker AP; Bocian M
Am J Med Genet; 1987 May; 27(1):3-22. PubMed ID: 3300332
[TBL] [Abstract][Full Text] [Related]
17. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
Schürmann M; Wethling H; Niemeyer ML; Schwinger E
Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
[TBL] [Abstract][Full Text] [Related]
18. De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.
Bonthron DT; Smith SJ; Fantes J; Gosden CM
Am J Hum Genet; 1993 Sep; 53(3):629-37. PubMed ID: 8352273
[TBL] [Abstract][Full Text] [Related]
19. Cri du chat-syndrome in combination with partial trisomy 9 p.
Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
[TBL] [Abstract][Full Text] [Related]
20. Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome.
Dallapiccola B; Bollea G; Mazzilli C; Gandini E
Hum Genet; 1976 Jul; 33(1):73-6. PubMed ID: 939560
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
