119 related articles for article (PubMed ID: 4134455)
1. Letter: Turner's syndrome and long-arm deletions of X chromosome.
Slater R; Ntuyabaliwe WK
Lancet; 1974 Jul; 2(7871):57-8. PubMed ID: 4134455
[No Abstract] [Full Text] [Related]
2. Letter: X long-arm deletion with features of Turner's syndrome.
Jenkins MB; O'Rourke WJ
Lancet; 1974 Feb; 1(7850):210. PubMed ID: 4129890
[No Abstract] [Full Text] [Related]
3. Letter: X long-arm deletion with features of Turner's syndrome.
Wright EV; Scanlon MF
Lancet; 1974 May; 1(7863):933. PubMed ID: 4133455
[No Abstract] [Full Text] [Related]
4. Letter: X long-arm deletion with features of Turner's syndrome.
Forabosco A; Dallapiccola B
Lancet; 1974 Aug; 2(7877):403-4. PubMed ID: 4137037
[No Abstract] [Full Text] [Related]
5. Letter: Long-arm deletion with features of Turner's syndrome.
Kim HJ; Hsu LY; Hirschhorn K
Lancet; 1974 Jun; 1(7869):1296. PubMed ID: 4134188
[No Abstract] [Full Text] [Related]
6. Turner's syndrome and 46,X,i(Yq) karyotype.
Magnelli NC; Vianna-Morgante AM; Frota-Pessoa O; Taboada-Lopez MG
J Med Genet; 1974 Dec; 11(4):403-6. PubMed ID: 4443992
[TBL] [Abstract][Full Text] [Related]
7. Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq).
Yanagisawa S; Yokoyama H
Clin Genet; 1975 Apr; 7(4):299-303. PubMed ID: 47795
[TBL] [Abstract][Full Text] [Related]
8. [Karyological variants in Turner's syndrome].
Zanoio L; Povia P; Amantea P
Minerva Ginecol; 1978 Oct; 30(10):817-20. PubMed ID: 724156
[No Abstract] [Full Text] [Related]
9. [Isochromosome X with long branches in two patients with Turner's syndrome].
Nikezić M; Jokanović R; Ajdarić B; Garzicić B; Necić S
Srp Arh Celok Lek; 1978 May; 106(5):553-61. PubMed ID: 751241
[No Abstract] [Full Text] [Related]
10. X-X translocation in a patient with Turner's syndrome.
Van den Berghe H; Fryns JP; Soyez C
Humangenetik; 1973 Dec; 20(4):377-80. PubMed ID: 4768115
[No Abstract] [Full Text] [Related]
11. [Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)].
Emerit I; German J; Crippa LP; Sureau C
Ann Genet; 1970 Dec; 13(4):245-8. PubMed ID: 5313888
[No Abstract] [Full Text] [Related]
12. Unusual abnormal X chromosome in hyperthyroidism and Turner's syndrome.
Chang JC; Burkle JS
N Y State J Med; 1973 May; 73(9):1101-4. PubMed ID: 4512169
[No Abstract] [Full Text] [Related]
13. An isodicentric X chromosome with gonadal dysgenesis in a lady without prominent somatic features of Turner's syndrome. A case report.
Yu TY; Lin HS; Chen PL; Huang TS
J Formos Med Assoc; 2015 Jan; 114(1):77-80. PubMed ID: 25618587
[TBL] [Abstract][Full Text] [Related]
14. Cytogenetic findings in 125 patients with Turner's syndrome and abnormal karyotypes.
Coco R; Bergada C
J Genet Hum; 1977 Jun; 25(2):95-107. PubMed ID: 915489
[TBL] [Abstract][Full Text] [Related]
15. Partial short arm deletion of the X chromosome 46,X,del(X)(qter = to p21:).
Käosaar M; Mikelsaar AV
Hum Genet; 1980 Feb; 53(2):275-7. PubMed ID: 7358395
[TBL] [Abstract][Full Text] [Related]
16. [Some remarks about the relation between the clinical picture of Turner's syndrome and a certain chromosome pattern].
Körner H
Zentralbl Gynakol; 1968 Dec; 90(50):1696-700. PubMed ID: 5708967
[No Abstract] [Full Text] [Related]
17. [2 cases of Turner's syndrome with diverse chromosome patterns; one 44 A-XO, the other 44 A-XisoX on the long arms].
Giovannucci ML; Pierro U; Calandi C; Casini Raggi G
Haematologica; 1969; 54(11):763-94. PubMed ID: 4993249
[No Abstract] [Full Text] [Related]
18. [Turner's syndrome with ring-shaped x chromosome].
Luciani JM; Arroyo H; Carlon N; Aubert L; Stahl A
Sem Hop; 1971 Dec; 47(52):2977-86. PubMed ID: 4334461
[No Abstract] [Full Text] [Related]
19. X/X translocation and Turner's syndrome in a woman with climacterium praecox.
Nielsen J; Kristoffersen E; Homma A
Acta Obstet Gynecol Scand; 1979; 58(3):309-12. PubMed ID: 484225
[TBL] [Abstract][Full Text] [Related]
20. Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi).
Ferguson-Smith MA; Boyd E; Ferguson-Smith ME; Pritchard JG; Yusuf AF; Gray B
J Med Genet; 1969 Dec; 6(4):422-5. PubMed ID: 5365951
[No Abstract] [Full Text] [Related]
[Next] [New Search]