126 related articles for article (PubMed ID: 27625830)
1. Different chromosome Y abnormalities in a case with short stature.
Balkan M; Fidanboy M; Özbek MN; Alp MN; Budak T
J Pediatr Genet; 2012 Dec; 1(4):239-42. PubMed ID: 27625830
[TBL] [Abstract][Full Text] [Related]
2. Different chromosome Y abnormalities in Turner syndrome.
Bağci G; Acar H; Tomruk H
Genet Couns; 2001; 12(3):255-61. PubMed ID: 11693789
[TBL] [Abstract][Full Text] [Related]
3. Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.
Castro A; Rodríguez F; Flórez M; López P; Curotto B; Martínez D; Maturana A; Lardone MC; Palma C; Mericq V; Ebensperger M; Cassorla F
Hum Reprod; 2017 Feb; 32(2):465-475. PubMed ID: 28057878
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Tetrasomy Y by structural rearrangement: clinical report.
DesGroseilliers M; Lemyre E; Dallaire L; Lemieux N
Am J Med Genet; 2002 Sep; 111(4):401-4. PubMed ID: 12210299
[TBL] [Abstract][Full Text] [Related]
6. Chromosome abnormalities in Indonesian patients with short stature.
Paramayuda C; Kartapradja H; Ambarwati DD; Anggaratri HW; Suciati LP; Marzuki NS; Harahap A
Mol Cytogenet; 2012 Aug; 5(1):35. PubMed ID: 22863325
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic and molecular analysis of a Yq isochromosome.
Guttenbach M; Müller U; Schmid M
Hum Genet; 1990 Dec; 86(2):147-50. PubMed ID: 2265826
[TBL] [Abstract][Full Text] [Related]
8. A Rare Mosaic Karyotype of 45,X/46,X,psu idic(Y)(p11.32)/46,XY with SHOX Haploinsufficiency, External Male Genitalia, and Short Stature.
Ekici C; Esener Z; Korkmaz S; Saltürk N; Yüksel S; Koç A
Sex Dev; 2019; 13(1):41-46. PubMed ID: 30504706
[TBL] [Abstract][Full Text] [Related]
9. Fluorescence in situ hybridization analysis of sex-chromosome mosaicism in azoospermic men.
Okada H; Dobashi M; Yamazaki T; Fujisawa M; Arakawa S; Kamidono S
J Androl; 2001; 22(6):970-2. PubMed ID: 11700861
[TBL] [Abstract][Full Text] [Related]
10. The use of fluorescence in situ hybridization in the diagnosis of hidden mosaicism: apropos of three cases of sex chromosome anomalies.
Maciel-Guerra AT; Paulo JD; Santos AP; Guaragna-Filho G; Andrade JG; Siviero-Miachon AA; Spinola-Castro AM; Guerra-Júnior G
Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):545-51. PubMed ID: 23295296
[TBL] [Abstract][Full Text] [Related]
11. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.
Bergendi E; Plöchl E; Vlasak I; Rittinger O; Muss W
Klin Padiatr; 1997; 209(3):133-6. PubMed ID: 9183775
[TBL] [Abstract][Full Text] [Related]
12. [Down-Turner syndrome (45,X/47,XY,+21): case report and review].
Ryu SW; Lee G; Baik CS; Shim SH; Kim JT; Lee JS; Lee KA
Korean J Lab Med; 2010 Apr; 30(2):195-200. PubMed ID: 20445340
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic and molecular characterization of two isodicentric Y chromosomes.
Stankiewicz P; Hélias-Rodzewicz Z; Jakubów-Durska K; Bocian E; Obersztyn E; Rappold GA; Mazurczak T
Am J Med Genet; 2001 Jun; 101(1):20-5. PubMed ID: 11343332
[TBL] [Abstract][Full Text] [Related]
14. Mosaic down syndrome with a marker: molecular cytogenetic characterization of the marker chromosome.
Dutta UR; Pidugu VK; Goud V; Dalal AB
Gene; 2012 Mar; 495(2):199-204. PubMed ID: 22245181
[TBL] [Abstract][Full Text] [Related]
15. A Novel Sex Chromosome Mosaicism 45,X/45,Y/46,XY/46,YY/47,XYY Causing Ambiguous Genitalia.
Khan MR; Bukhari I; Junxiang T; Hui L; Muhammad N; Fan C; Zhu J; Wu M
Ann Clin Lab Sci; 2017 Nov; 47(6):761-764. PubMed ID: 29263053
[TBL] [Abstract][Full Text] [Related]
16. Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development.
Dutta UR; Pidugu VK; Goud ChV; Hoefers C; Hagemann M; Dalal A
Gene; 2013 May; 519(2):374-80. PubMed ID: 23428792
[TBL] [Abstract][Full Text] [Related]
17. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
Huang Y; Sun X; Li Q
Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
[TBL] [Abstract][Full Text] [Related]
18. Molecular‑cytogenetic study of de novo mosaic karyotype 45,X/46,X,i(Yq)/46,X,idic(Yq) in an azoospermic male: Case report and literature review.
Jiang Y; Wang R; Li L; Xue L; Deng S; Liu R
Mol Med Rep; 2017 Sep; 16(3):3433-3438. PubMed ID: 28713994
[TBL] [Abstract][Full Text] [Related]
19. FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.
Kirsch S; Weiss B; De Rosa M; Ogata T; Lombardi G; Rappold GA
J Med Genet; 2000 Aug; 37(8):593-9. PubMed ID: 10922386
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic and molecular characterization of Y isochromosome in a 63XO/64Xi(Yq) mosaic karyotype of an intersex horse.
Das PJ; Lyle SK; Beehan D; Chowdhary BP; Raudsepp T
Sex Dev; 2012; 6(1-3):117-27. PubMed ID: 22005008
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
