Heterozygous deletion at 14g22.1-g22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

Heterozygous deletion at 14g22.1-g22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly
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14g22.1-g22.3 杂合缺失,包括精神运动迟缓、先天性角膜混浊和足多指并指患者的 BMP4 基因

DOI:
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发表时间:
2008
期刊:
Am J Med Genet A 146A
影响因子:
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通讯作者:
et.al.
et.al.
中科院分区:
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文献类型:
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作者:
Hayashi S;et.al.

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