162 related articles for article (PubMed ID: 505084)
1. A teen-ager with 46,X,del(X)(q21).
Srivastava PK; Fristoe F; McDavid RE; Townsend JF
South Med J; 1979 Nov; 72(11):1461-3. PubMed ID: 505084
[TBL] [Abstract][Full Text] [Related]
2. Primary amenorrhea with a new mosaic 46,XXqi/47,XXqi Xp-. Consideration on the X isochromosome formation and X chromosome inactivation.
Halbrecht I; Shabtai F; Kuperstain C
Acta Genet Med Gemellol (Roma); 1977; 26(1):63-9. PubMed ID: 71839
[TBL] [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. Partial long arm deletion of one X chromosome in a patient with secondary amenorrhea.
Ruthner U; Maschik S; Friedrich F; Breitenecker G
Hum Genet; 1979 Apr; 48(1):135-7. PubMed ID: 457129
[TBL] [Abstract][Full Text] [Related]
5. X-X translocation in a patient with gonadal dysgenesis and the problems of phenotype-karyotype correlations.
Mirzayants GG; Baranovskaya LI
Hum Genet; 1978 Feb; 40(3):249-57. PubMed ID: 631846
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosome.
de la Chapelle A; Grönman P; Latt SA
Cytogenet Cell Genet; 1978; 20(1-6):204-12. PubMed ID: 348409
[TBL] [Abstract][Full Text] [Related]
8. An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome.
Barnes IC; Curtis DJ; Duncan SL
J Med Genet; 1987 Jul; 24(7):428-31. PubMed ID: 3612719
[TBL] [Abstract][Full Text] [Related]
9. A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea.
Branković S; Laća Z; Dramusić V; Ivanović M; Morić-Petrović S
Hum Genet; 1979 Apr; 48(1):139-42. PubMed ID: 457130
[TBL] [Abstract][Full Text] [Related]
10. Isodicentric X chromosome in a woman with characteristics of gonadal dysgenesis.
Laća Z; Ivanović M; Dramusić V; Morić-Petrović S
Hum Genet; 1979 Jun; 49(2):237-41. PubMed ID: 468255
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic study of primary amenorrhoea.
Roy AK; Banerjee D
J Indian Med Assoc; 1995 Aug; 93(8):291-2. PubMed ID: 8713239
[TBL] [Abstract][Full Text] [Related]
12. [Cytogenetic studies in primary amenorrhea].
Baron J; Warenik-Szymankiewicz A
Zentralbl Gynakol; 1975; 97(11):649-55. PubMed ID: 1189755
[TBL] [Abstract][Full Text] [Related]
13. Familial occurrence of isodicentric X chromosomes with different breakpoints.
Midro AT; Kulikowski M; Sawicka A; Panasiuk B; Korsak E
Clin Genet; 1988 Sep; 34(3):153-60. PubMed ID: 3180502
[TBL] [Abstract][Full Text] [Related]
14. [Sex chromosome aberrations in patients with menstruation disorders].
Midro AT; Panasiuk B; Radwan J; Sipowicz I; Jaworowska B; Korsak E
J Gynecol Obstet Biol Reprod (Paris); 1990; 19(7):811-6. PubMed ID: 2277162
[TBL] [Abstract][Full Text] [Related]
15. Short arm deletion of an X chromosome, 46,XXp-.
Kaiser P; Zabel B; Hansen S; Daume E
Hum Genet; 1976 Apr; 32(1):89-100. PubMed ID: 1262028
[TBL] [Abstract][Full Text] [Related]
16. [Iso-X chromosomes in primary amenorrhoea and Turner's syndrome - presentation by C-banding (author's transl)].
Zernahle K
Zentralbl Gynakol; 1980; 102(3):151-60. PubMed ID: 7211028
[TBL] [Abstract][Full Text] [Related]
17. [xXi karyotype and Turner's syndrome].
Broustet A; Nogue F; Emperaire JC; Garcia J; Darmaillacq R
Bord Med; 1972 Mar; 5(6):679-84. PubMed ID: 4560010
[No Abstract] [Full Text] [Related]
18. [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]
19. Cytogenetic and clinical study on 100 cases of primary amenorrhoea.
Kallio H
Acta Obstet Gynecol Scand Suppl; 1973; ():1-78. PubMed ID: 4518464
[No Abstract] [Full Text] [Related]
20. Familial x/x translocation: t(x;x)(p22;q13).
Kim HJ; Hsu LY; Hirschhorn K
Cytogenet Cell Genet; 1974; 13(5):454-64. PubMed ID: 4462981
[No Abstract] [Full Text] [Related]
[Next] [New Search]
