232 related articles for article (PubMed ID: 15849801)
1. Y chromosome heterochromatin of differing lengths in two cell populations of the same individual.
Akkari Y; Lawce H; Kelson S; Smith C; Davis C; Boyd L; Magenis RE; Olson S
Prenat Diagn; 2005 Apr; 25(4):304-6. PubMed ID: 15849801
[TBL] [Abstract][Full Text] [Related]
2. [Intra-individual polymorphism of human Y chromosome as a result of deletion in the heterochromatin region].
Nazarenko SA; Nazarenko LP; Baranova VA
Genetika; 1987 May; 23(5):918-21. PubMed ID: 3623089
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.
Hwa HL; Ko TM; Chang YY; Huang CH; Su YN; Tseng LH; Hsieh FJ
Prenat Diagn; 2004 Feb; 24(2):121-4. PubMed ID: 14974120
[TBL] [Abstract][Full Text] [Related]
4. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
5. Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report.
Pinho MJ; Neves R; Costa P; Ferrás C; Sousa M; Alves C; Almeida C; Fernandes S; Silva J; Ferrás L; Barros A
Hum Reprod; 2005 Mar; 20(3):689-96. PubMed ID: 15665019
[TBL] [Abstract][Full Text] [Related]
6. Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up.
Marchina E; Piovani G; Vezzola L; Bellotti D; Cerri V; Groli C; Barlati S
Prenat Diagn; 2003 Dec; 23(12):959-63. PubMed ID: 14663830
[TBL] [Abstract][Full Text] [Related]
7. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
[TBL] [Abstract][Full Text] [Related]
8. Two extra euchromatic bands in the qh region of chromosome 9.
Ozkinay F; Ercal D; Ozkinay C; Onay H; Bora E; Erler A
Genet Couns; 2005; 16(1):45-8. PubMed ID: 15844778
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of mosaic tetrasomy 5p.
Park JP; Barefoot KH; Ornvold K; Berg SZ; Dossu JR; Mohandas TK
Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
[TBL] [Abstract][Full Text] [Related]
10. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
[TBL] [Abstract][Full Text] [Related]
11. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.
Sawyer JR; Swanson CM; Wheeler G; Cunniff C
Am J Med Genet; 1995 Mar; 56(2):203-9. PubMed ID: 7625446
[TBL] [Abstract][Full Text] [Related]
12. Y chromosome heterochromatin variation detected at prenatal diagnosis.
Cotter PD; Norton ME
Prenat Diagn; 2005 Nov; 25(11):1062-3. PubMed ID: 16299832
[No Abstract] [Full Text] [Related]
13. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
Iourov IY; Vorsanova SG; Liehr T; Monakhov VV; Soloviev IV; Yurov YB
Cytogenet Genome Res; 2008; 121(3-4):302-6. PubMed ID: 18758177
[TBL] [Abstract][Full Text] [Related]
14. Comparison of two techniques for transcervical cell sampling performed in the same study population.
Cioni R; Bussani C; Scarselli B; Bucciantini S; Marchionni M; Scarselli G
Prenat Diagn; 2005 Mar; 25(3):198-202. PubMed ID: 15791667
[TBL] [Abstract][Full Text] [Related]
15. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
16. Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies.
Bashamboo A; Rahman MM; Prasad A; Chandy SP; Ahmad J; Ali S
Mol Hum Reprod; 2005 Feb; 11(2):117-27. PubMed ID: 15579656
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.
Chien SC; Chen CP; Lin CC; Huang LC; Hsieh CT; Tsai FJ
Taiwan J Obstet Gynecol; 2009 Sep; 48(3):292-5. PubMed ID: 19797023
[TBL] [Abstract][Full Text] [Related]
18. Mosaic ring Y chromosome in two normal healthy men with azoospermia.
Bertini V; Canale D; Bicocchi MP; Simi P; Valetto A
Fertil Steril; 2005 Dec; 84(6):1744. PubMed ID: 16359976
[TBL] [Abstract][Full Text] [Related]
19. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
20. Prenatal detection of a de novo Yqh-acrocentric translocation.
Ng LK; Kwok YK; Tang LY; Ng PP; Ghosh A; Lau ET; Tang MH
Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
