203 related articles for article (PubMed ID: 58062)
1. Familial 'partial 9p' trisomy: six cases and four carriers in three generations.
Centerwall WR; Miller KS; Reeves LM
J Med Genet; 1976 Feb; 13(1):57-61. PubMed ID: 58062
[TBL] [Abstract][Full Text] [Related]
2. The trisomy 9p syndrome.
Centerwall WR; Beatty-DeSana JW
Pediatrics; 1975 Nov; 56(5):748-55. PubMed ID: 1196731
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
Wang XR; Luo RL; Dai XH; Liu JY
Yi Chuan; 2007 Jul; 29(7):813-6. PubMed ID: 17646146
[TBL] [Abstract][Full Text] [Related]
6. A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).
Mason MK; Spencer DA; Rutter A
J Med Genet; 1975 Sep; 12(3):310-4. PubMed ID: 1177287
[TBL] [Abstract][Full Text] [Related]
7. Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.
Zaremba J; Zdzienicka E; Glogowska I; Abramowicz T; Taracha B
J Ment Defic Res; 1974 Jun; 18(2):153-90. PubMed ID: 4141378
[No Abstract] [Full Text] [Related]
8. [Familial observation of partial trisomy 6, and probable partial monosomy 18q by parental translocation].
D'Emma C; Crippa L; Delozier C; Michail E; Graber P
J Genet Hum; 1982 Mar; 30(1):39-50. PubMed ID: 7130955
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).
Habedank M; Faust J
Hum Genet; 1978 Jun; 42(3):251-6. PubMed ID: 149755
[TBL] [Abstract][Full Text] [Related]
10. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
Butomo IV; Prozorova MV; Khitrikova LE
Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
[TBL] [Abstract][Full Text] [Related]
11. Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11).
Carnevale A; Frías S; del Castillo V
Clin Genet; 1978 Oct; 14(4):202-6. PubMed ID: 699358
[TBL] [Abstract][Full Text] [Related]
12. Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).
Penehaszadeh VB; Coco R
J Med Genet; 1975 Sep; 12(3):301-5. PubMed ID: 1177284
[TBL] [Abstract][Full Text] [Related]
13. A case of trisomy 9p in a family with translocation 9/15.
Balícek P; Zizka J; Lichý J
Humangenetik; 1975; 27(4):353-8. PubMed ID: 1150257
[No Abstract] [Full Text] [Related]
14. Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.
Slinde S; Hansteen IL
Eur J Pediatr; 1982 Oct; 139(2):153-7. PubMed ID: 7151837
[TBL] [Abstract][Full Text] [Related]
15. Trisomy for the distal half of the short arm of chromosome 9. A variant of the trisomy 9p syndrome.
Lewandowski RC; Yunis JJ; Lehrke R; O'Leary J; Swaiman KF; Sanchez O
Am J Dis Child; 1976 Jun; 130(6):663-7. PubMed ID: 937286
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.
Sandig KR; Mücke J; Veit H
Hum Genet; 1979 Nov; 52(2):175-8. PubMed ID: 511173
[TBL] [Abstract][Full Text] [Related]
17. Genetic risks for familial reciprocal translocations with special emphasis on those leading to 9p, 10p and 12p trisomies.
Stene J; Stengel-Rutkowski S
Ann Hum Genet; 1982 Jan; 46(1):41-74. PubMed ID: 7103412
[TBL] [Abstract][Full Text] [Related]
18. Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.
Williams JD; Summitt RL; Martens PR; Kimbrell RA
Am J Hum Genet; 1975 Jul; 27(4):478-85. PubMed ID: 125542
[TBL] [Abstract][Full Text] [Related]
19. A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation.
Mulcahy MT; Jenkyn J; Masters PL
Clin Genet; 1974; 6(5):335-40. PubMed ID: 4434650
[No Abstract] [Full Text] [Related]
20. A new case of the trisomy 9P syndrome. Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p) and a peculiar congenital heart defect.
Orye E; Verhaaren H; Van Egmond H; Devloo-Blancquaert A
Clin Genet; 1975 Feb; 7(2):134-43. PubMed ID: 1132161
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
