184 related articles for article (PubMed ID: 4752865)
1. Reciprocal translocation versus centric fusion between two No. 13 chromosomes. A case of 46,XX,-13,+t(13;13)(p12;q13) and a case of 46,XY,-13,+t(13;13)(p12;p12).
Hsu LY; Kim HJ; Sujansky E; Kousseff B; Hirschhorn K
Cytogenet Cell Genet; 1973; 12(4):235-44. PubMed ID: 4752865
[No Abstract] [Full Text] [Related]
2. New chromosomal syndromes.
Lewandowski RC; Yunis JJ
Am J Dis Child; 1975 Apr; 129(4):515-29. PubMed ID: 124130
[No Abstract] [Full Text] [Related]
3. [Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].
Stoll C; Halb A
Pediatrie; 1974; 29(7):725-9. PubMed ID: 4456285
[No Abstract] [Full Text] [Related]
4. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)].
Menéndez I; Casaña H
Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884
[TBL] [Abstract][Full Text] [Related]
5. Partial trisomy 13 in a case of Cyclopia with 13-14 translocation.
Singh DN; Wiscovitch RA; Osborne RA; Hennigar GR
Clin Genet; 1974; 5(3):218-22. PubMed ID: 4209592
[No Abstract] [Full Text] [Related]
6. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22).
Rivera H; Rivas F; Plascencia L; Cantú JM
Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704
[TBL] [Abstract][Full Text] [Related]
7. Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence.
Yu FC; Gutman LT; Huang SW; Fresh JW; Emanuel I
J Med Genet; 1970 Jun; 7(2):132-7. PubMed ID: 5519598
[No Abstract] [Full Text] [Related]
8. Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome.
Abe T; Morita M; Kawai K; Misawa S; Kanai H; Hirose G; Fujita H
Humangenetik; 1975 Sep; 30(3):207-15. PubMed ID: 1184006
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
Wilroy RS; Summitt RL; Martens P; Gooch WM
Ann Genet; 1977 Dec; 20(4):237-42. PubMed ID: 305749
[TBL] [Abstract][Full Text] [Related]
11. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
Cantu JM; Salamanca F; Buentello L; Carnevale A; Armendares S
Ann Genet; 1975 Mar; 18(1):5-11. PubMed ID: 1080038
[TBL] [Abstract][Full Text] [Related]
12. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations.
Hasegawa T; Hasegawa Y; Asamura S; Nagai T; Tsuchiya Y; Ninomiya M; Fukushima Y
Clin Genet; 1991 Sep; 40(3):202-6. PubMed ID: 1773535
[TBL] [Abstract][Full Text] [Related]
13. Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy.
Kaye CI; Booth CW; Meeker D; Nadler HL
Cleft Palate J; 1977 Jul; 14(3):244-8. PubMed ID: 267527
[TBL] [Abstract][Full Text] [Related]
14. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
Butler LJ; Eades SM; France NE
Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
[No Abstract] [Full Text] [Related]
15. 46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3.
Surana RB; Braudo ME; Conen PE; Slade RH
Clin Genet; 1977 Mar; 11(3):201-6. PubMed ID: 837571
[No Abstract] [Full Text] [Related]
16. Partial trisomy 13q inherited from balanced translocation (5;13) (p14;q13).
Coco R; del Rey G
J Genet Hum; 1978 Dec; 26(4):303-10. PubMed ID: 752064
[TBL] [Abstract][Full Text] [Related]
17. [Trisomy due to transmitted translocation t(13 q , 14 q ). Estimation of recurrence risks].
Belaisch G; Despres P; Plainfosse B; Rethore O; Emerit I; Loewe-Lyon S; Lejeune J; Seringe P
Arch Fr Pediatr; 1971 Oct; 28(8):865-74. PubMed ID: 5123542
[No Abstract] [Full Text] [Related]
18. An unusual partial trisomy 13.
Stoll C; Messer J; Weitzenblum S; Warter S
Clin Genet; 1976 Jan; 9(1):1-4. PubMed ID: 813920
[No Abstract] [Full Text] [Related]
19. 3:1 meiotic disjunction in a mother with a balanced translocation, 46,XX,t(5,14)(p15;q13) resulting in tertiary trisomy and tertiary monosomy offspring.
Abeliovich D; Yagupsky P; Bashan N
Am J Med Genet; 1982 May; 12(1):83-9. PubMed ID: 7091199
[No Abstract] [Full Text] [Related]
20. Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies.
Golbus MS; Conte FA; Daentl DL
J Med Genet; 1973 Mar; 10(1):83-5. PubMed ID: 4121427
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
