308 related articles for article (PubMed ID: 6705241)
1. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
van de Vooren MJ; Planteydt HT; Hagemeijer A; Peters-Slough MF; Timmerman MJ
Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
[TBL] [Abstract][Full Text] [Related]
2. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8)(p15.3;p22). Case report, review and risk estimates.
Stengel-Rutkowski S; Warkotsch A; Schimanek P; Stene J
Clin Genet; 1984 Jun; 25(6):500-21. PubMed ID: 6539659
[TBL] [Abstract][Full Text] [Related]
3. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
[TBL] [Abstract][Full Text] [Related]
4. Ring (13),t(2;6) associated with familial fragile (16).
Ventruto V; Rinaldi A; Renda S; Stabile M; Rinaldi MM; Cavaliere ML; Conte N; Aveta V
J Med Genet; 1984 Jun; 21(3):233. PubMed ID: 6748026
[No Abstract] [Full Text] [Related]
5. 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]
6. Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).
Fonatsch C; Flatz SD
Humangenetik; 1974; 25(3):227-33. PubMed ID: 4141336
[No Abstract] [Full Text] [Related]
7. Five generations of t(4;8)(q35;q13) leading to a case of partial 8q trisomy with consideration of potential pregnancy outcomes from translocation carriers.
Young RS; Hansen KL; Khodr GS
Clin Genet; 1984 Jun; 25(6):522-7. PubMed ID: 6733948
[TBL] [Abstract][Full Text] [Related]
8. Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23).
Chieri P; Iölster N
Clin Genet; 1983 Aug; 24(2):147-50. PubMed ID: 6616953
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Severe mental retardation in a boy with partial trisomy 10q and partial monosomy 2q.
Sills JA; Buckton KE; Raeburn JA
J Med Genet; 1976 Dec; 13(6):507-10. PubMed ID: 1018309
[TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
Stoll C; Levy J; Roth MP
J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
[TBL] [Abstract][Full Text] [Related]
12. Partial trisomy 12q: report of a case and review.
Roberts SH; Mattina T; Laurence KM; Sorge G; Pavone L
J Med Genet; 1981 Dec; 18(6):470-3. PubMed ID: 7334509
[TBL] [Abstract][Full Text] [Related]
13. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
Sartori A; Tenconi R; Baccichetti C; Pujatti G
Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
[No Abstract] [Full Text] [Related]
14. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
[No Abstract] [Full Text] [Related]
15. 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]
16. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
Taysi K; Chao WT; Monaghan N; Monaco MP
Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
[TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 7p in two families resulting from different balanced translocations.
Moore CM; Pfeiffer RA; Craig-Holmes AP; Scott CI; Meisel-Stosiek M
Clin Genet; 1982 Feb; 21(2):112-21. PubMed ID: 7083611
[No Abstract] [Full Text] [Related]
18. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.
Hobolth N; Jacobsen P; Mikkelsen M
J Med Genet; 1974 Sep; 11(3):299-303. PubMed ID: 4139263
[TBL] [Abstract][Full Text] [Related]
19. Familial translocation t(10;21)(q22;q22).
Delicado A; Pajares IL; Vicente P; Hawkins F
Hum Genet; 1979 Sep; 50(3):253-8. PubMed ID: 489009
[TBL] [Abstract][Full Text] [Related]
20. Interstitial deletion of the short arm of chromosome 4.
Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]