Turner's syndrome with interstitial and presumptive terminal deletion short arm X.

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作者信息

Sillesen I, Rasmussen K, Nielsen J

出版信息

Hereditas. 1976;84(1):123-5. doi: 10.1111/j.1601-5223.1976.tb01202.x.

DOI:10.1111/j.1601-5223.1976.tb01202.x

PMID:1010756

Abstract

摘要

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Turner's syndrome with interstitial and presumptive terminal deletion short arm X.

Hereditas. 1976;84(1):123-5. doi: 10.1111/j.1601-5223.1976.tb01202.x.

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Endokrynol Pol. 1977 May-Jun;28(3):255-60.

Letter: X long-arm deletion with features of Turner's syndrome.

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Turner's syndrome and 46,X,i(Yq) karyotype.

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引用本文的文献

Inactivation centers in the human X chromosome.

Am J Hum Genet. 1982 Mar;34(2):182-94.

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相似文献

Turner's syndrome with interstitial and presumptive terminal deletion short arm X.

Hereditas. 1976;84(1):123-5. doi: 10.1111/j.1601-5223.1976.tb01202.x.

[Ring chromosome in Turner's syndrome with a 45,X/46,X,Xr mosaic].

Endokrynol Pol. 1977 May-Jun;28(3):255-60.

Letter: X long-arm deletion with features of Turner's syndrome.

Lancet. 1974 May 11;1(7863):933. doi: 10.1016/s0140-6736(74)90385-7.

Letter: X long-arm deletion with features of Turner's syndrome.

Lancet. 1974 Feb 9;1(7850):210. doi: 10.1016/s0140-6736(74)92509-4.

Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq).

Clin Genet. 1975 Apr;7(4):299-303. doi: 10.1111/j.1399-0004.1975.tb00332.x.

Letter: X long-arm deletion with features of Turner's syndrome.

Lancet. 1974 Aug 17;2(7877):403-4. doi: 10.1016/s0140-6736(74)91781-4.

Letter: Long-arm deletion with features of Turner's syndrome.

Lancet. 1974 Jun 22;1(7869):1296. doi: 10.1016/s0140-6736(74)90062-2.

X del(q) Turner's syndrome in a 30-month-old girl.

Hum Hered. 1977;27(5):356-61. doi: 10.1159/000152890.

Triple mosaicism of the sex chromosomes in Turner's syndrome and Hirschsprung's disease.

Lancet. 1961 Sep 16;2(7203):623-7. doi: 10.1016/s0140-6736(61)90307-5.

Turner's syndrome and 46,X,i(Yq) karyotype.

J Med Genet. 1974 Dec;11(4):403-6. doi: 10.1136/jmg.11.4.403.

引用本文的文献

Inactivation centers in the human X chromosome.

Am J Hum Genet. 1982 Mar;34(2):182-94.