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Results: 1 to 20 of 101

1.

AZFc deletion detected in a newborn with prenatally diagnosed Yq deletion.

Tóth A, Tardy EP, Gombos S, Hajdu K, Bátorfi J, Krausz C.

Prenat Diagn. 2001 Apr;21(4):253-5.

PMID:
11288112
[PubMed - indexed for MEDLINE]
2.

Cytogenetic and molecular analysis of male infertility: Y chromosome deletion during nonobstructive azoospermia and severe oligozoospermia.

Dada R, Gupta NP, Kucheria K.

Cell Biochem Biophys. 2006;44(1):171-7.

PMID:
16456245
[PubMed - indexed for MEDLINE]
3.

Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.

Velissariou V, Antoniadi T, Patsalis P, Christopoulou S, Hatzipouliou A, Donoghue J, Bakou K, Kaminopetros P, Athanassiou V, Petersen MB.

Prenat Diagn. 2001 Jun;21(6):484-7.

PMID:
11438955
[PubMed - indexed for MEDLINE]
4.

Yq deletions and AZF locus: molecular analysis in two fetuses with non familial homogeneous Yq rearrangements.

Camurri L, Novelli G, Gennarelli M, Cantarelli M, Dallapicolla B.

Genet Couns. 1993;4(3):223-6.

PMID:
8267932
[PubMed - indexed for MEDLINE]
5.

Five cases of prenatally diagnosed sex chromosome mosaicism.

Nocera G, Dalpra' L, Tibiletti MG, Buscaglia M.

Prenat Diagn. 1985 May-Jun;5(3):169-74.

PMID:
4022940
[PubMed - indexed for MEDLINE]
6.

Prenatal identification of i(Yp) by molecular cytogenetic analysis.

Wang BB, Yu LC, Peng W, Falk RE, Williams J 3rd.

Prenat Diagn. 1995 Dec;15(12):1115-9.

PMID:
8750290
[PubMed - indexed for MEDLINE]
7.

Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection.

Kent-First M, Muallem A, Shultz J, Pryor J, Roberts K, Nolten W, Meisner L, Chandley A, Gouchy G, Jorgensen L, Havighurst T, Grosch J.

Mol Reprod Dev. 1999 May;53(1):27-41.

PMID:
10230814
[PubMed - indexed for MEDLINE]
8.

[Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].

Ulmer R, Pfeiffer RA, Kollert A, Beinder E.

Z Geburtshilfe Neonatol. 2000 Jan-Feb;204(1):1-7. German.

PMID:
10721179
[PubMed - indexed for MEDLINE]
9.

Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe.

Disteche C, Luthy D, Haslam DB, Hoar D.

Hum Genet. 1984;67(2):222-4.

PMID:
6745944
[PubMed - indexed for MEDLINE]
10.

Sex chromosome mosaicism in males carrying Y chromosome long arm deletions.

Siffroi JP, Le Bourhis C, Krausz C, Barbaux S, Quintana-Murci L, Kanafani S, Rouba H, Bujan L, Bourrouillou G, Seifer I, Boucher D, Fellous M, McElreavey K, Dadoune JP.

Hum Reprod. 2000 Dec;15(12):2559-62.

PMID:
11098026
[PubMed - indexed for MEDLINE]
Free Article
11.

Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia.

Zhou-Cun A, Yang Y, Zhang SZ, Zhang W, Lin L.

Yi Chuan Xue Bao. 2006 Feb;33(2):111-6.

PMID:
16529294
[PubMed - indexed for MEDLINE]
12.

Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

Margarit E, Soler A, Carrió A, Oliva R, Costa D, Vendrell T, Rosell J, Ballesta F.

J Med Genet. 1998 Sep;35(9):727-30.

PMID:
9733030
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

[Microdeletion of Y chromosome in severe olygozoospemic infertile patient].

Castro A, López P, Johnson MC, Sovino H, Martínez C, Vantman D.

Rev Med Chil. 2000 Jul;128(7):778-82. Spanish.

PMID:
11050840
[PubMed - indexed for MEDLINE]
14.

Prenatal identification of an isochromosome for the short arm of the Y i(Yp), by cytogenetic and molecular analyses.

Slim R, Soulié J, Hotmar J, Lecolier B, Bercau G, Bernheim A.

Prenat Diagn. 1994 Jan;14(1):23-8.

PMID:
8183834
[PubMed - indexed for MEDLINE]
15.

Prenatal identification of mos 45,X/46,X,+mar in a normal male baby by cytogenetic and molecular analysis.

Hoshi N, Tonoki H, Handa Y, Fujino T, Okuyama K, Koga Y, Matsumoto Y, Yamada T, Yamada H, Kishida T, Sagawa T, Fujieda K, Nakahori Y, Kant JA, Fujimoto S.

Prenat Diagn. 1998 Dec;18(12):1316-22.

PMID:
9885026
[PubMed - indexed for MEDLINE]
16.

Fine mapping of re-arranged Y chromosome in three infertile patients with non-obstructive azoospermia/cryptozoospermia.

Faure AK, Aknin-Seifer I, Satre V, Amblard F, Devillard F, Hennebicq S, Chouteau J, Bergues U, Levy R, Rousseaux S.

Hum Reprod. 2007 Jul;22(7):1854-60.

PMID:
17582144
[PubMed - indexed for MEDLINE]
Free Article
17.

[Molecular cytogenetic studies of 25 males with azoospermia].

Ge YS, Zhou YL, Wu HN.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Apr;25(2):190-4. Chinese.

PMID:
18393244
[PubMed - indexed for MEDLINE]
18.

Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.

Valetto A, Bertini V, Rapalini E, Baldinotti F, Di Martino D, Simi P.

Fertil Steril. 2004 May;81(5):1388-90.

PMID:
15136108
[PubMed - indexed for MEDLINE]
20.

Genetic risk factors in infertile men with severe oligozoospermia and azoospermia.

Dohle GR, Halley DJ, Van Hemel JO, van den Ouwel AM, Pieters MH, Weber RF, Govaerts LC.

Hum Reprod. 2002 Jan;17(1):13-6.

PMID:
11756355
[PubMed - indexed for MEDLINE]
Free Article

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