A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation.

A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation.

The potential of a new fluorescent in situ hybridization technique is discussed, which uses a complete set of telomeric probes to reveal cryptic chromosome rearrangements that remain undetected by standard cytogenetic analysis. We report the obstetric history of a patient who had a termination of pr...

書誌詳細
主要な著者:	Brackley, K, Kilby, MD, Morton, J, Whittle, M, Knight, S, Flint, J
フォーマット:	Journal article
言語:	English
出版事項:	1999

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