一个患有15/16平衡易位的家族中的16号染色体三体。 - Suppr

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16q trisomy in a family with a balanced 15/16 translocation.

作者信息

Schmickel R, Poznanski A, Himebaugh J

出版信息

Birth Defects Orig Artic Ser. 1975;11(5):229-36.

PMID:1218219

Abstract

摘要

相似文献

16q trisomy in a family with a balanced 15/16 translocation.

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引用本文的文献

Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report.

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Trisomy 16q21 = to qter.

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Trisomy 16q13----qter in a infant from a t(11;16)(q25;q13) translocation-carrier father.

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Partial trisomy 16p due to maternal balanced translocation.

J Med Genet. 1984 Aug;21(4):315-6. doi: 10.1136/jmg.21.4.315.

Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

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Trisomy 16q23----qter arising from a maternal t(13;16)(p12;q23): case report and evidence of the reciprocal balanced maternal rearrangement by the Ag-NOR technique.

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Partial trisomy 16q-.

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Partial monosomy of the long arm of chromosome 16 in a malformed newborn: karyotype 46,XX,del(16))q21).

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Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.

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