遗传性X连锁铁利用障碍性贫血。两种Xg血型和卟啉含量不同的红细胞群体的分离。 - Suppr

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超能文献

Hereditary, X-linked, sideroachrestic anemia. The isolation of two erythrocyte populations differing in Xga blood type and porphyrin content.

作者信息

Lee G R, MacDiarmid W D, Cartwright G E, Wintrobe M M

出版信息

Blood. 1968 Jul;32(1):59-70.

PMID:5658391

Abstract

摘要

相似文献

Hereditary, X-linked, sideroachrestic anemia. The isolation of two erythrocyte populations differing in Xga blood type and porphyrin content.遗传性X连锁铁利用障碍性贫血。两种Xg血型和卟啉含量不同的红细胞群体的分离。

Blood. 1968 Jul;32(1):59-70.

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引用本文的文献

The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene.X染色体上的人类双糖链蛋白聚糖基因BGN会发生X染色体失活，但它的转录方式却如同X-Y同源基因。

Hum Genet. 1995 Jul;96(1):44-52. doi: 10.1007/BF00214185.

Sideroblastic anaemia. A review of seven paediatric cases.铁粒幼细胞贫血。7例儿科病例综述。

Eur J Pediatr. 1982 Mar;138(2):130-5. doi: 10.1007/BF00441138.

X-chromosome inactivation and the Xg locus.X染色体失活与Xg血型位点

Am J Hum Genet. 1970 Jul;22(4):460-3.

Genetics of protan and deutan color-vision anomalies: an instructive family.红色盲和绿色盲色觉异常的遗传学：一个有指导意义的家族。

Am J Hum Genet. 1969 Nov;21(6):581-92.

The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry.X连锁血型系统Xg。对北欧血统的无血缘关系个体及家族的检测。

J Med Genet. 1971 Dec;8(4):427-33. doi: 10.1136/jmg.8.4.427.

Xg groups and sex abnormalities in people of northern European ancestry.北欧血统人群中的Xg血型组与性异常

J Med Genet. 1971 Dec;8(4):417-26. doi: 10.1136/jmg.8.4.417.

Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder.遗传性铁粒幼细胞贫血和共济失调：一种X连锁隐性疾病。

J Med Genet. 1985 Aug;22(4):267-73. doi: 10.1136/jmg.22.4.267.

5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia.5-氨基酮戊酸合酶位于3p21，因此不是X连锁铁粒幼细胞贫血的主要缺陷。

Am J Hum Genet. 1988 Sep;43(3):331-5.

X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.X连锁铁粒幼细胞贫血伴共济失调：与位于Xq13的磷酸甘油酸激酶基因连锁

Am J Hum Genet. 1991 Feb;48(2):335-41.

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