144 related articles for article (PubMed ID: 837573)
1. The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction.
Bergamo F; Crosato F; Francesconi D; Pasqual F; Zuffardi O
Clin Genet; 1977 Mar; 11(3):219-23. PubMed ID: 837573
[TBL] [Abstract][Full Text] [Related]
2. The 9p- deletion syndrome. Report of a patient with a 46, XX, 9P- constitution due to a paternal t(9p-;15+) translocation.
Orye E; Verhaaren H; Van den Bogaert-Van Heesvelde AM
Clin Genet; 1975 Nov; 8(5):349-57. PubMed ID: 1204232
[TBL] [Abstract][Full Text] [Related]
3. Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7.
Winsor EJ; Palmer CG; Ellis PM; Hunter JL; Ferguson-Smith MA
Cytogenet Cell Genet; 1978; 20(1-6):169-84. PubMed ID: 648176
[TBL] [Abstract][Full Text] [Related]
4. Complex chromosomal rearrangement involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32----qter.
Al-Awadi SA; Teebi AS; Sundareshan TS
Ann Genet; 1985; 28(3):181-4. PubMed ID: 3879154
[TBL] [Abstract][Full Text] [Related]
5. The 12p trisomy syndrome.
Armendares S; Salamanca F; Nava S; Ramirez S; Cantu JM
Ann Genet; 1975 Jun; 18(2):89-94. PubMed ID: 1081370
[TBL] [Abstract][Full Text] [Related]
6. Trisomy 9p in a patient with a de novo 9/15 translocation.
Jacobsen P; Hobolth N; Mikkelsen M
Clin Genet; 1975 Apr; 7(4):317-24. PubMed ID: 1126053
[TBL] [Abstract][Full Text] [Related]
7. A clinical syndrome associated with 5p duplication and 9p deletion.
Liberfarb RM; Atkins L; Holmes LB
Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
[TBL] [Abstract][Full Text] [Related]
8. Concordant congenital malformations in twins with inherited translocation: t(9p--;13q+).
Sekhon GS; Taysi K
Hum Genet; 1979 Sep; 50(3):271-6. PubMed ID: 489011
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. 7q deletion syndrome (7q32 leads to 7qter).
Harris EL; Wappner RS; Palmer CG; Hall B; Dinno N; Seashore MR; Breg WR
Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
[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. A homologous tandem translocation [45,XX,-13,-13,+t(13;13) (q12;q34)].
Cohen MM; Rosen Y; Gadoth N; Tal A
Cytogenet Cell Genet; 1978; 20(1-6):155-9. PubMed ID: 648174
[TBL] [Abstract][Full Text] [Related]
13. Familial t(4;13) with abnormal offspring in three generations.
Najafzadeh TM; Littman VA; Dumars KW
Am J Med Genet; 1983 Sep; 16(1):15-22. PubMed ID: 6638065
[TBL] [Abstract][Full Text] [Related]
14. Presumptive long arm deletion of chromosome 8: a new syndrome?
Taysi K; Noetzel MJ; Strauss AW
Hum Genet; 1979 Sep; 51(1):49-53. PubMed ID: 500091
[TBL] [Abstract][Full Text] [Related]
15. Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter).
Franceschini P; Silengo MC; Davi GF; Santoro MA; Prandi G; Fabris C
Hum Genet; 1978 Nov; 44(3):345-8. PubMed ID: 730173
[TBL] [Abstract][Full Text] [Related]
16. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
[TBL] [Abstract][Full Text] [Related]
17. Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).
Schinzel A; Hayashi K; Schmid W
Humangenetik; 1975 Dec; 30(4):307-16. PubMed ID: 1218860
[TBL] [Abstract][Full Text] [Related]
18. Distal deletion of the short arm of chromosome No. 10: a case report.
Oka S; Nakano H; Yokochi T; Ueda K; Saito A
Jinrui Idengaku Zasshi; 1983 Dec; 28(4):291-6. PubMed ID: 6678316
[No Abstract] [Full Text] [Related]
19. 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]
20. 46,XX,-12,+der(12),rcp(3;12)(p25.1;p13.31)pat karyotype in a girl. Probable subregional assignment of glyceraldehyde-3-phosphate dehydrogenase locus to 12p13.1----p13.31 by exclusion mapping.
Rivas F; Vaca G; Zúñiga G; González RM; Ruiz C; Rivera H; Moller M; Cantu JM
Ann Genet; 1985; 28(3):189-92. PubMed ID: 3879156
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]