255 related articles for article (PubMed ID: 5314293)
1. A case of 18q- in a t(18q-;6p+) family.
Jacobsen P; Mikkelsen M; Niebuhr E; de Grouchy J
Ann Genet; 1971 Mar; 14(1):41-8. PubMed ID: 5314293
[No Abstract] [Full Text] [Related]
2. A family with a presumptive C-F translocation in five generations.
Therkelsen AJ; Klinge T; Henningsen K; Mikkelsen M; Schmidt G
Ann Genet; 1971 Mar; 14(1):13-21. PubMed ID: 5314290
[No Abstract] [Full Text] [Related]
3. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
[No Abstract] [Full Text] [Related]
4. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
Mikkelsen M; Niebuhr E
Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712
[No Abstract] [Full Text] [Related]
5. The 18p- syndrome. Report of two cases.
Jacobsen P; Mikkelsen M
Ann Genet; 1968 Dec; 11(4):211-6. PubMed ID: 5306362
[No Abstract] [Full Text] [Related]
6. [A case of translocation t(Cp-; Bp+)].
Ricci N; Ventimiglia B; Dallapiccola B; Preto G
Ann Genet; 1967 Jun; 10(2):82-5. PubMed ID: 5298977
[No Abstract] [Full Text] [Related]
7. [A new case of a ring shaped chromosome 18 (18 r)].
Petit P; Poncelet R
Ann Genet; 1967 Sep; 10(3):134-7. PubMed ID: 5300397
[No Abstract] [Full Text] [Related]
8. [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)].
Lejeune J; Berger R; Réthoré MO; Lafourcade J; Dutrillaux B; Canlorbe P; Labrune B
Ann Genet; 1967 Mar; 10(1):18-24. PubMed ID: 5300122
[No Abstract] [Full Text] [Related]
9. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child].
Walbaum R; Dupuis C; Dehaene P; Delmas-Marsalet Y
Ann Genet; 1968 Mar; 11(1):53-5. PubMed ID: 5301757
[No Abstract] [Full Text] [Related]
10. Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings.
Fraccaro M; Hulten M; Ivemark BI; Lindsten J; Tiepolo L; Zetterqvist P
Ann Genet; 1971 Dec; 14(4):275-80. PubMed ID: 5316132
[No Abstract] [Full Text] [Related]
11. 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]
12. Trisomy 4p in a family with A t(4;15).
Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ
Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034
[TBL] [Abstract][Full Text] [Related]
13. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).
Parker CE; Mavalwala J; Koch R; Hatashita A; Derencsenyi A
Calif Med; 1972 Oct; 117(4):65-71. PubMed ID: 5075725
[No Abstract] [Full Text] [Related]
14. [The 18q-syndrome. Deletion of the long arm of chromosome nr. 18].
Kroyer S; Niebuhr E; Vestermark S
Ugeskr Laeger; 1974 Apr; 136(15):827. PubMed ID: 4828093
[No Abstract] [Full Text] [Related]
15. [Familial occurrence of long arm deletion in chromosome 18 (46,18q-)].
Dziuba P; Jończyk K; Dziekanowska D; Bulsiewicz H
Pediatr Pol; 1972 Aug; 47(8):1037-42. PubMed ID: 5074000
[No Abstract] [Full Text] [Related]
16. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].
Gilgenkrantz S; Marchal C; Neimann N
Ann Genet; 1968 Mar; 11(1):17-21. PubMed ID: 5301751
[No Abstract] [Full Text] [Related]
17. Trisomy 18 associated with a familial translocation t(Bq-; 18q+).
France NE; Butler LJ
Ann Genet; 1969 Mar; 12(1):46-50. PubMed ID: 5306711
[No Abstract] [Full Text] [Related]
18. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
Smith GF; Shear CS; Jalowayski I; Akesson HO
J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
[No Abstract] [Full Text] [Related]
19. [The Dr syndrome. Study of a further case (46, XX, 14r)].
Gilgenkrantz S; Cabrol C; Lausecker C; Hartleyb ME; Bohe B
Ann Genet; 1971 Mar; 14(1):23-31. PubMed ID: 5314291
[No Abstract] [Full Text] [Related]
20. A case of 18q-in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding technique.
Gouw WL; ten Kate LP; Anders GJ; Okken A
Humangenetik; 1973; 19(1):123-6. PubMed ID: 4725908
[No Abstract] [Full Text] [Related]
[Next] [New Search]