132 related articles for article (PubMed ID: 728592)
1. Follow-up on a human X-autosome translocation first studied in 1963 and 1964.
Opitz JM; DeMars RI; Inhorn SL; Elejalde BR
Birth Defects Orig Artic Ser; 1978; 14(6C):365-75. PubMed ID: 728592
[No Abstract] [Full Text] [Related]
2. X-autosome translocations: a review.
Summitt RL; Tipton RE; Wilroy RS; Martens PR; Phelan JP
Birth Defects Orig Artic Ser; 1978; 14(6C):219-47. PubMed ID: 365268
[No Abstract] [Full Text] [Related]
3. 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]
4. 46, X, del (X) (p21) in a 14-year-old female with Turner signs, one streak and one normal ovary.
Crisalli M; Cuoco C; Gimelli G; Monteverde R
Ann Genet; 1981; 24(2):114-6. PubMed ID: 6977291
[No Abstract] [Full Text] [Related]
5. Pregnancy in five women with 45,X/46,XX and 45,X/47,XXX gonadal dysgenesis.
Shokeir MH
Birth Defects Orig Artic Ser; 1978; 14(6C):171-84. PubMed ID: 728581
[No Abstract] [Full Text] [Related]
6. Chromosomal diagnosis of the Werner syndrome.
Jaramillo C; Jorgenson RJ; Miles DA; Moore CM
Birth Defects Orig Artic Ser; 1985; 21(2):119-26. PubMed ID: 4041574
[No Abstract] [Full Text] [Related]
7. X inactivation pattern in an unbalanced X-autosome translocation with gonadal dysgenesis.
Gaál M; László J
Hum Hered; 1977; 27(6):396-402. PubMed ID: 908575
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
Bjerglund Nielsen L; Nielsen IM
Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482
[TBL] [Abstract][Full Text] [Related]
11. XX-XO complex of sex chromosomes in a child with an unusual phenotype.
Mikel'saar AV; Naidenova MM; Tal'vik TA; Mikel'saar RV; Kaselaid VL; Tsuker EI; Grinberg KN
Sov Genet; 1973 Aug; 7(2):250-5. PubMed ID: 4804067
[No Abstract] [Full Text] [Related]
12. An atypical Turner syndrome patient with ring X chromosome mosaicism.
Cantú ES; Jacobs DF; Pai GS
Ann Clin Lab Sci; 1995; 25(1):60-5. PubMed ID: 7762970
[TBL] [Abstract][Full Text] [Related]
13. The KOP translocation.
Pallister PD; Opitz JM
Birth Defects Orig Artic Ser; 1978; 14(6C):133-46. PubMed ID: 569514
[No Abstract] [Full Text] [Related]
14. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
Canún S; Mutchinick O; Shaffer LG; Fernández C
Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
[TBL] [Abstract][Full Text] [Related]
15. Replication patterns of three isodicentric X chromosomes and an X isochromosome in human lymphocytes.
Dewald G; Spurbeck JL; Gordon H
Am J Med Genet; 1978; 1(4):445-60. PubMed ID: 665728
[TBL] [Abstract][Full Text] [Related]
16. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
Hsu LY
Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
[TBL] [Abstract][Full Text] [Related]
17. PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.
Osipova GR; Karmanov ME; Kozlova SI; Evgrafov OV
Am J Med Genet; 1998 Apr; 76(4):283-7. PubMed ID: 9545090
[TBL] [Abstract][Full Text] [Related]
18. Turner syndrome and 45,X/47,XXX mosaicism.
Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
[TBL] [Abstract][Full Text] [Related]
19. Non-fluorescent Y-chromosome.
Bühler EM; Bühler UK; Tsuchimoto T; Stalder GR
Helv Paediatr Acta; 1974 Nov; 29(5):447-56. PubMed ID: 4141700
[No Abstract] [Full Text] [Related]
20. A boy with true hermaphroditism and sex chromosome mosaicism and a fertile woman with Turner mosaicism in a family with a translocation 8p:19P.
Annerén G; Frykberg T; Gustavson KH
Clin Genet; 1981 Oct; 20(4):289-95. PubMed ID: 7333022
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
