Article

Klinefelter Syndrome with Azoospermia：Identiﬁcation of a Neocentromic Y Chromosome with No Detectable DYZ3 Centromeric Sequence

2021-01-15

Abstract excerpt

<title>Abstract</title> <p><bold>Background </bold>Individuals with rare cytogenetic variants have contributed to our understanding of the genetics of sex chromosome and its disorders. Here, we report on a 23 years old man with a de novo 47,XX,+mar.ish der(Y)neo(Y)(pter-->p11.2::q11.23-->neo-->q11.23-->qter)(DYZ3-,SRY+,WCPY+) chromosome complement, accompanying with azoospermia and some of other clinical features...

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Literature Corpus work: 3a68673b-6535-5434-a07e-4b85a40eda6d
DOI: 10.21203/rs.3.rs-146030/v1

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Klinefelter Syndrome with Azoospermia：Identiﬁcation of a Neocentromic Y Chromosome with No Detectable DYZ3 Centromeric SequenceDOI 10.21203/rs.3.rs-146030/v1Read

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