164 related articles for article (PubMed ID: 2570022)
1. Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry.
Cooke A; Tolmie JL; Colgan JM; Greig CM; Connor JM
Hum Genet; 1989 Aug; 83(1):83-7. PubMed ID: 2570022
[TBL] [Abstract][Full Text] [Related]
2. Jumping translocation in a newborn boy with dup(4q) and severe hydrops fetalis.
Duval E; van den Enden A; Vanhaesebrouck P; Speleman F
Am J Med Genet; 1994 Aug; 52(2):214-7. PubMed ID: 7802011
[TBL] [Abstract][Full Text] [Related]
3. MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/14q duplication.
Fryns JP; Borghgraef M; Lemmens F; van den Berghe H
Clin Genet; 1993 Sep; 44(3):146-8. PubMed ID: 8275573
[TBL] [Abstract][Full Text] [Related]
4. A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat.
el-Rifai W; Leisti J; Kähkönen M; Pietarinen A; Altherr MR; Knuutila S
J Med Genet; 1995 Jan; 32(1):65-7. PubMed ID: 7897631
[TBL] [Abstract][Full Text] [Related]
5. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities].
Gregori Romero M; Gil Benso R; López Ginés C; Pellín Pérez A; Barberá Guillem E
An Esp Pediatr; 1984 Oct; 21(6):593-6. PubMed ID: 6524770
[TBL] [Abstract][Full Text] [Related]
6. Low level mosaicism for a balanced 7;14 translocation in the father of an abnormal 7q+ child.
Sciorra LJ; Schlenker E; Toke D; Brady-Yasbin S; Day-Salvatore D; Lee ML
Am J Med Genet; 1992 Feb; 42(3):296-7. PubMed ID: 1536164
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
Zackowski JL; Raffel LJ; McDaniel LD; Schwartz S
Ann Genet; 1990; 33(2):113-6. PubMed ID: 2241085
[TBL] [Abstract][Full Text] [Related]
10. Familial translocation t(10;14) (q26.1;q32.3): report of three offspring with 10q deletion and 14q duplication.
Huang TH; Peckham D; Batanian JR; Martin MB; Kouba M; Caldwell CW; Miles JH
Clin Genet; 1994 Oct; 46(4):299-303. PubMed ID: 7834895
[TBL] [Abstract][Full Text] [Related]
11. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
[TBL] [Abstract][Full Text] [Related]
12. Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat.
Moedjono SJ; Sparkes RS
Hum Genet; 1979 Sep; 50(3):241-6. PubMed ID: 489007
[TBL] [Abstract][Full Text] [Related]
13. Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.
Summitt RL; Tharapel AT; Wilroy RS
Eur J Pediatr; 1977 Jul; 125(3):169-74. PubMed ID: 885143
[TBL] [Abstract][Full Text] [Related]
14. Complex chromosome rearrangements and congenital anomalies.
Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
[TBL] [Abstract][Full Text] [Related]
15. A balanced complex chromosomal rearrangement (BCCR) with phenotypic effect.
Del Porto G; Grammatico P; De Sanctis S; Esposito M; Di Rosa C; Romano C
Clin Genet; 1991 Jul; 40(1):57-61. PubMed ID: 1884518
[TBL] [Abstract][Full Text] [Related]
16. Williams syndrome and chromosome 18.
Menko FH; Stouthart PJ
J Med Genet; 1992 Sep; 29(9):679-80. PubMed ID: 1404306
[No Abstract] [Full Text] [Related]
17. De novo translocation involving chromosomes 2, 8, and 20.
Zaletajev DV; Marincheva GS; Tsvetkova TG
J Med Genet; 1984 Jun; 21(3):231. PubMed ID: 6748024
[No Abstract] [Full Text] [Related]
18. The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred.
Francke U; Jones KL
Am J Dis Child; 1976 Nov; 130(11):1244-9. PubMed ID: 984008
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Complex rearrangement of chromosomes 3 and 5 in an adolescent with multiple abnormalities].
Naffah J; Der Kaloustian V
Ann Genet; 1975 Jun; 18(2):121-4. PubMed ID: 242250
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
