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Items: 1 to 20 of 96

1.

D-E (13-15/17-18) translocation: occurrence in an infant with 45 chromosomes.

Townes PL, Ziegler NA.

Am J Dis Child. 1965 Dec;110(6):686-8. No abstract available.

PMID:
5845212
2.

[Familial D-E translocation].

Meyer-Robisch M, Schwanitz G.

Acta Genet Med Gemellol (Roma). 1967 Oct;16(4):365-75. German. No abstract available.

PMID:
5593928
3.

Familial D-E translocation.

Orye E, Van Nevel C.

Humangenetik. 1968;6(3):191-9. No abstract available.

PMID:
5709078
4.

A family with D-D translocation.

Krmpotic E, Ramanathan K, Grossman A.

J Med Genet. 1968 Sep;5(3):205-10. No abstract available.

5.

Three unusual trisomic patterns in children. Triple X plus triple E-triple X mosaic: normal XY-D trisomy mosaic; partial trisomy with E translocation.

Engel E, Haddow JE, Lewis JF, Tipton RE, Overall JC, McGee BJ, Levrat OJ, Engel-de-montmollin M.

Am J Dis Child. 1967 Mar;113(3):322-8. No abstract available.

PMID:
6019450
6.

Siblings with different types of chromosal aberrations due to D-E-translocation of the mother.

Hauschteck E, Mürset G, Prader A, Bühler E.

Cytogenetics. 1966;5(5):281-94. No abstract available.

PMID:
6006217
7.

[Trisomy 10p as a result of familial 10/22 translocation].

Zergollern L, Begovic D, Muzinić D.

Acta Med Iugosl. 1980;34(2):113-22. Croatian. No abstract available.

PMID:
7405617
8.

The ascertainment and implications of an unbalanced translocation in the neonate. Familial 1:15 translocation.

Hain D, Leversha M, Campbell N, Daniel A, Barr PA, Rogers JG.

Aust Paediatr J. 1980 Sep;16(3):196-200. No abstract available.

PMID:
7224998
9.

Congenital acute lymphoblastic leukemia with chromosomal abnormalities including a translocation (1;4;22).

Gilgenkrantz S, Benz E, Chiclet AM, Buisine J, Gregoire MJ, Olive D, Vinet E, Streiff F.

Cancer Genet Cytogenet. 1983 Sep;10(1):37-42.

PMID:
6576852
10.
11.

4;11 translocation in acute lymphoblastic leukemia: a specific syndrome.

Morse HG, Heideman R, Hays T, Robinson A.

Cancer Genet Cytogenet. 1982 Oct;7(2):165-72. No abstract available.

PMID:
6959693
12.

A family showing transmission of a translocation between a 6-12 chromosome and a 21-22 chromosome.

Gray JE, Dartnall JA, Macnamara BG.

J Med Genet. 1966 Mar;3(1):62-5. No abstract available.

13.

[Trisomy 10 p. Apropos of a case caused by a maternal translocation].

Stoll C, Willard D.

Pediatrie. 1980 Apr-May;35(3):251-5. French. No abstract available.

PMID:
7393692
14.

[Genetic prognosis of chromosome translocations].

Srsen S, Volna J.

Cesk Pediatr. 1980 Apr;35(4):196-203. Slovak. No abstract available.

PMID:
7397898
15.

Case of hereditary (4;5) translocation discovered prenatally.

Sun NH, Wang FY, Li JX, Zhou XT.

Chin Med J (Engl). 1981 Sep;94(9):597-600. No abstract available.

PMID:
6793325
16.

Karyotype-phenotype correlation in partial trisomy 13. Report of a case due to maternal translocation.

Bonioli E, Crisalli M, Monteverde R, Vianello MG.

Am J Dis Child. 1981 Dec;135(12):1115-7.

PMID:
7315808
17.

De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

López-Pajares I, Martin-Ancel A, Cabello P, Delicado A, Garcia-Alix A, San Roman C.

Clin Genet. 1993 Feb;43(2):94-7.

PMID:
8448910
18.

[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. Spanish.

PMID:
8442884
19.

[12 p trisomy. A new case (author's transl)].

Kubryk N, Prieur M, Borde M.

Ann Pediatr (Paris). 1980 Dec;27(10):695-9. French. No abstract available.

PMID:
7212558
20.

[A case of C-D translocation in a 9 year old boy and his mother].

Revazov AA, Russkikh VV.

Tsitologiia. 1966 Mar-Apr;8(2):269-76. Russian. No abstract available.

PMID:
5984073

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