136 related articles for article (PubMed ID: 6499261)
1. Maternal translocation t(13:18)(q34:q11) and Edward's syndrome in a fetus: 47,xy,t(13:18)(q34:q11) + 18.
Marković S; Boué J; Krstić M; Sulović V; Dozić S; Adzić S
Clin Genet; 1984 Nov; 26(5):481-4. PubMed ID: 6499261
[TBL] [Abstract][Full Text] [Related]
2. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11).
Murthy DS; Patel ZM; Ambani LM
Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 18(q11 leads to qter) in an infant and aborted fetus resulting from a balanced paternal translocation t(13;18)(q32:q11).
Rosenmann A; Isacson M; Cohen R; Segal M; Cohen MM
Ann Genet; 1978 Mar; 21(1):60-4. PubMed ID: 308346
[TBL] [Abstract][Full Text] [Related]
4. Maternal autosomal translocation t(5;18)(q12;q11) and Edward's syndrome in the fetus.
Fryns JP
Clin Genet; 1985 Nov; 28(5):397. PubMed ID: 4085144
[No Abstract] [Full Text] [Related]
5. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
Cohen MM; Ornoy A; Rosenmann A; Kohn G
Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
[TBL] [Abstract][Full Text] [Related]
6. Tertiary trisomy, 47,XX,+14q--, resulting from maternal balanced translocation, 46,XX,t(14;16)(q11;q24).
Young SR; Donovan DM; Greer HA; Burch K; Potter DC
Hum Genet; 1976 Aug; 33(3):331-4. PubMed ID: 964994
[TBL] [Abstract][Full Text] [Related]
7. Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.
Stern LM; Mureh AR
J Med Genet; 1975 Sep; 12(3):305-7. PubMed ID: 1177285
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of partial trisomy 22 derived from a maternal t(11; 22) (q23; q11).
Sou S; Takabayashi T; Sasaki H; Sasamoto K; Shintaku Y; Li ZJ; Ozawa N; Yajima A
Tohoku J Exp Med; 1987 Dec; 153(4):389-93. PubMed ID: 3441929
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16)(p12;q11).
Nevin NC; Coffey WW; Nevin J; Reid MM
Clin Genet; 1983 Nov; 24(5):375-9. PubMed ID: 6652947
[TBL] [Abstract][Full Text] [Related]
10. [Chromosomes and fertility. Translocation 13:15 and 13:18 and spontaneous abortion].
Adzić S; Mijin K; Sulović V; Marković S; Krstić M
Jugosl Ginekol Opstet; 1981; 21(1-2):23-5. PubMed ID: 7052393
[TBL] [Abstract][Full Text] [Related]
11. Partial trisomy 16p due to maternal balanced translocation.
McMorrow LE; Bornstein S; Fischer RH; Gluckson MM
J Med Genet; 1984 Aug; 21(4):315-6. PubMed ID: 6492098
[TBL] [Abstract][Full Text] [Related]
12. Partial monosomy 13q and partial trisomy 18p: case report with necropsy findings.
Beneck D; Greco MA; Wolman SR; McMorrow LE; Jansen V; Cason J
J Med Genet; 1986 Jun; 23(3):260-3. PubMed ID: 3723557
[TBL] [Abstract][Full Text] [Related]
13. Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.
Rosi G; Venti G; Migliorini Brushelli G; Donti E; Bocchini V; Armellini R
Hum Genet; 1979 Sep; 51(1):67-72. PubMed ID: 500094
[TBL] [Abstract][Full Text] [Related]
14. A case of Edward's syndrome with pseudodicentric isochromosome 18: 46,XY,i dic(18) (p11::p11).
Fioretti G; Stabile M; Pagano L; Rinaldi A; Rolando D; Trapassi C; de Tollis G; Ventruto V
Ann Genet; 1982; 25(2):116-8. PubMed ID: 6984627
[No Abstract] [Full Text] [Related]
15. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
Fryns JP; Casaer P; Van den Berghe H
Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
[TBL] [Abstract][Full Text] [Related]
16. Two new chromosomal abnormalities in chronic myelogenous leukemia 46,XY,t(9;15;22)(q34;q22;q11) and 46,XY,t(6;9;12;22)(p21;q34;q24;q11).
Ramirez GM; Macera MJ; Verma RS
Cancer Genet Cytogenet; 1989 Mar; 38(1):115-9. PubMed ID: 2713807
[TBL] [Abstract][Full Text] [Related]
17. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
[TBL] [Abstract][Full Text] [Related]
18. Fetal phenotype in a case of partial trisomy 21 and partial monosomy 22 detected prenatally.
Migliorini AM; Coco R; De Negrotti TC; Sanchez JM; Castineyra G
J Med Genet; 1981 Oct; 18(5):383-5. PubMed ID: 6460105
[TBL] [Abstract][Full Text] [Related]
19. Familial 5/14 translocation with triple X and 47,XY + 14q.
Lancet M; Sindel L; Segal I
Clin Genet; 1981 Jul; 20(1):40-3. PubMed ID: 7296947
[TBL] [Abstract][Full Text] [Related]
20. [Partial trisomy 18 (pter leads to q122) of maternal origin (author's transl)].
Jaffray JY; Geneix A; Goumy P; Perissel B; Menut G; Malet P
Ann Genet; 1980; 23(4):224-7. PubMed ID: 6971601
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
