164 related articles for article (PubMed ID: 953214)
1. X short-arm deletion gonadal dysgenesis in two sibs.
Davis JR; Heine MW; Graap RF; Lightner ES; Giles HR
Birth Defects Orig Artic Ser; 1976; 12(5):137-8. PubMed ID: 953214
[No Abstract] [Full Text] [Related]
2. X/X translocation in a girl with gonadal dysgenesis.
Ishitobi K; Harada R; Ninomiya T; Santo Y; Harada Y
Yonago Acta Med; 1976 Apr; 20(1):19-27. PubMed ID: 1025924
[No Abstract] [Full Text] [Related]
3. X-short arm deletion gonadal dysgenesis in two siblings due to unique translocation (Xp-;16p+).
Davis JR; Heine MW; Lightner ES; GILES HR; Graap RF
Clin Genet; 1976 Oct; 10(4):202-7. PubMed ID: 975595
[TBL] [Abstract][Full Text] [Related]
4. The Turner phenotype associated with unbalanced X/autosome translocation.
Leisti J; Kaback MM; Rimoin DL
Birth Defects Orig Artic Ser; 1975; 11(5):315-7. PubMed ID: 1218231
[No Abstract] [Full Text] [Related]
5. [Y chromosome structural abnormalities and Turner's syndrome].
Ravel C; Siffroi JP
Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
[TBL] [Abstract][Full Text] [Related]
6. [Familial X-autosomal translocation t (X, 2)].
Mashkova MV; Verlinskaia DK
Tsitologiia; 1976 Jul; 18(7):901-5. PubMed ID: 982591
[TBL] [Abstract][Full Text] [Related]
7. [Gonadal dysgenesis with ring-shaped chromosome in an adolescent girl].
Voog R; Jalbert P; Chambaz E; Hadjian A; Pallo D; Grubier M; Perdrix A; Lachaud P
Sem Hop; 1971 Dec; 47(52):2965-75. PubMed ID: 4334460
[No Abstract] [Full Text] [Related]
8. [Partial short arm deletion of x chromosome and Turner stigmata: report of a case and review of the literature].
Ishitobi K; Watanabe A; Miyagi S; Harada Y; Nakada N
Nihon Naika Gakkai Zasshi; 1982 Sep; 71(9):1275-82. PubMed ID: 7153629
[No Abstract] [Full Text] [Related]
9. Gonadal dysgenesis in association with autosomal chromosome aberration.
Shapiro LR; Graves ZR; Warburton D; Huss HA
Birth Defects Orig Artic Ser; 1978; 14(6C):167-70. PubMed ID: 728580
[No Abstract] [Full Text] [Related]
10. [Chromatin-positive gonadal dysgenesis].
Aspillaga M; Avendaño I; Aguirre MI; Labraña C
Rev Chil Pediatr; 1986; 57(6):542-5. PubMed ID: 3671830
[No Abstract] [Full Text] [Related]
11. Gonosomal aberrations and congenital dyschromatopsias.
François J
Mod Probl Ophthalmol; 1974; 13(0):231-47. PubMed ID: 4548140
[No Abstract] [Full Text] [Related]
12. Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data.
Simpson JL; Christakos AC; Horwith M; Silverman FS
Birth Defects Orig Artic Ser; 1971 May; 7(6):215-28. PubMed ID: 5173165
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [X chromosome with deletion of the long arm].
Gilgenkrantz S; Baué G
J Gynecol Obstet Biol Reprod (Paris); 1977; 6(3):337-45. PubMed ID: 903575
[TBL] [Abstract][Full Text] [Related]
15. Dicentric X-isochromosome (Xqi dic) and pericentric inversion of No. 2 [inv(2) (p15 q21)] in a patient with gonadal dysgenesis.
Cohen MM; Rosenmann A; Hacham-Zadeh S; Dahan S
Clin Genet; 1975 Jul; 8(1):11-7. PubMed ID: 1149316
[TBL] [Abstract][Full Text] [Related]
16. X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere.
Maraschio P; Scappaticci S; Ferrari E; Fraccaro M
Ann Genet; 1977 Sep; 20(3):179-83. PubMed ID: 304701
[TBL] [Abstract][Full Text] [Related]
17. [Unusual autosome alterations in a case of gonadal dysgenesis accomplanied by short stature without deformations].
Salti F; Montali E; Conti C; Guazzelli R; Bigozzi U
Arch De Vecchi Anat Patol; 1968 Dec; 54(1):105-8. PubMed ID: 5744063
[No Abstract] [Full Text] [Related]
18. [Identification of a dicentric isochromosome (X dic qi) in a case of gonadal dysgenesis].
Colle ML; Byrd RJ
Pediatrie; 1977 Jun; 32(4):383-8. PubMed ID: 887359
[No Abstract] [Full Text] [Related]
19. 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]
20. [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]
[Next] [New Search]
