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

Prenatal Diagnosis

Volumn 21, Issue 6, 2001, Pages 484-487

  Velissariou, Voula ^a   Antoniadi, Thalia ^a   Patsalis, Philippos ^b   Christopoulou, Stavroula ^a   Hatzipouliou, Athina ^a   Donoghue, Jackie ^a   Bakou, Katerina ^a   Kaminopetros, Petros ^c   Athanassiou, Vassilis ^a   Petersen, Michael B ^a  

^a Gastroenterology Department   (Greece)

^b CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

^c NONE   (Greece)

Author keywords

AZF loci; Deletion Yq; Prenatal diagnosis; Satellited Yqs; Y chromosome structural aberrations

Indexed keywords

ADULT; ARTICLE; AZOOSPERMIA; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION Y; CHROMOSOME STRUCTURE; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE AMPLIFICATION; GENE LOCUS; HUMAN; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADULT; CHROMOSOME DELETION; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; POLYMERASE CHAIN REACTION; PREGNANCY; PREGNANCY TRIMESTER, FIRST; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; Y CHROMOSOME;

EID: 0034912676     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.79     Document Type: Article

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