与先天性异常相关的4号染色体长臂缺失（46,XX,4q-）

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Partial monosomy of long arm of chromosome 4 due to interstitial deletion.

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The partial 4q monosomy. Report of a 5-year-old boy with deletion 4q31.3 leads to 4qter.

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A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.

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Interstitial deletion of chromosome 4q diagnosed prenatally.

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Renal and urinary tract abnormalities associated with chromosome aberrations.

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Pericentric inversion and partial monosomy 4q associated with congenital anomalies.

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Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies.

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