152 related articles for article (PubMed ID: 5682047)
1. [Deficiency at the short arm of chromosome No. 18 (46, XX, 18p-). A uniform abnormality syndrome].
Reinwein H; Struwe FE; Bettecken F; Wolf U
Monatsschr Kinderheilkd (1902); 1968 Sep; 116(9):511-4. PubMed ID: 5682047
[No Abstract] [Full Text] [Related]
2. A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
Parker CE; Donnell GN; Mavalwala J; Hurst N; Derencsenyi A
Clin Pediatr (Phila); 1973 Jan; 12(1):42-6. PubMed ID: 4345621
[No Abstract] [Full Text] [Related]
3. Partial deletion of the long arm of chromosome E-18.
Curran JP; al-Salihi FL; Allderdice PW
Pediatrics; 1970 Nov; 46(5):721-9. PubMed ID: 5481073
[No Abstract] [Full Text] [Related]
4. A case with short arm deletion of chromosome 18 (18p-syndrome).
Kumagai M; Kikuchi Y; Oishi H; Matsuda E; Kato J
Jinrui Idengaku Zasshi; 1973 Jun; 18(1):24-36. PubMed ID: 4796358
[No Abstract] [Full Text] [Related]
5. A patient with a short arm deletion of chromosome 18 (46,XY,18p-).
Weiss L; Mayeda K
J Med Genet; 1969 Jun; 6(2):216-9. PubMed ID: 5801470
[No Abstract] [Full Text] [Related]
6. Chromosome 18 abnormalities in a family with a translocation t(18p--, 21p+).
Jacobsen P; Mikkelsen M
J Ment Defic Res; 1968 Jun; 12(2):144-61. PubMed ID: 5663940
[No Abstract] [Full Text] [Related]
7. [18p-Syndrome. Deletion of the short arm of chromosome 18].
Jacobsen P
Ugeskr Laeger; 1973 Jan; 135(1):17. PubMed ID: 4684842
[No Abstract] [Full Text] [Related]
8. [Deficiency of the long arm of chromosome no. 18 (46,XX,18q-)].
Cenani A; Schoeller L; Schubart G
Arch Kinderheilkd; 1969 Mar; 178(3):266-72. PubMed ID: 5800650
[No Abstract] [Full Text] [Related]
9. Trisomy 18.
James AE; Belcourt CL; Atkins L; Janower ML
Radiology; 1969 Jan; 92(1):37-43. PubMed ID: 4236175
[No Abstract] [Full Text] [Related]
10. Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.
Fischer P; Golob E; Friedrich F; Kunze-Mühl E; Doleschel W; Aichmair H
J Med Genet; 1970 Mar; 7(1):91-8. PubMed ID: 5480972
[No Abstract] [Full Text] [Related]
11. [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]
12. Familial transmission of a presumptive D/E (13-15/17-18) short arm translocation.
Cohen MM; Lockwood MA
Pediatr Res; 1967 Mar; 1(2):104-9. PubMed ID: 6029809
[No Abstract] [Full Text] [Related]
13. [Tetrasomy of the short arm of human chromosome 18: cytogenetics and phenotypic disorders].
Kuleshov NP; Zaletaev DV; Levina LIa; Dement'eva GM; Arbuzov SP
Tsitol Genet; 1985; 19(6):452-6. PubMed ID: 4089954
[TBL] [Abstract][Full Text] [Related]
14. A human ring D chromosome associated with multiple congenital abnormalities.
Teplitz RL; Miller D; Hansson KM; Rundall TS
J Pediatr; 1967 Jun; 70(6):936-41. PubMed ID: 6026119
[No Abstract] [Full Text] [Related]
15. Tetrasomy 18p: a distinctive syndrome.
Rivera H; Möller M; Hernández A; Enríquez-Guerra MA; Arreola R; Cantú JM
Ann Genet; 1984; 27(3):187-9. PubMed ID: 6334486
[TBL] [Abstract][Full Text] [Related]
16. [Rare case of mosaicism for chromosome 18, karyotype: 46, XX, del(18) (p11)/46, XX, i(18q)].
Badalian LO; Mutovin GR; Malygina NA; Petrukhin AS
Genetika; 1983 Nov; 19(11):1912-5. PubMed ID: 6686175
[TBL] [Abstract][Full Text] [Related]
17. D/E translocation in a young girl.
Miller JQ; Selden RF; Meisner LF
South Med J; 1970 Apr; 63(4):368-70. PubMed ID: 5437582
[No Abstract] [Full Text] [Related]
18. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
Vivarelli R; Paolieri M; Anichini C; Scarinci R; Berardi R; Rosaia L; Pucci L
Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
[TBL] [Abstract][Full Text] [Related]
19. Partial deletion of short arm of chromosome 18.
Kiss P; Osztovics M; Kosztolányi G; Papp A
Acta Paediatr Hung; 1984; 25(3):263-9. PubMed ID: 6498007
[TBL] [Abstract][Full Text] [Related]
20. Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.
Parker CE; Koch R; Mavalwala J; Derencsenyi A; Hatashita A
Clin Pediatr (Phila); 1969 Aug; 8(8):453-8. PubMed ID: 5797429
[No Abstract] [Full Text] [Related]
[Next] [New Search]