Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report

X chromosome deletion is an infrequent finding in prenatal diagnosis and presents a difficult counseling challenge when it occurs. We present a case of a familial X chromosome long arm deletion discovered in a routine amniocentesis and subsequently in the mother. The pregnancy resulted in the birth...

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Veröffentlicht in:Prenatal diagnosis 2001-01, Vol.21 (1), p.27-30
Hauptverfasser: Brown, Lucia Y., Alonso, M. Lita, Yu, Judy, Warburton, Dorothy, Brown, Stephen
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Sprache:eng
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