[伴有不同类型不平衡子代的遗传性易位t(4号染色体长臂缺失；18号染色体长臂增加)(作者译)] - Suppr

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超能文献

[Inherited translocation t(4q minus;18q plus) with unbalanced progeny of different types (author's transl)].

作者信息

Knörr-Gärtner H, Knörr K, Haas B, Vogel W, Siebers J W

出版信息

Humangenetik. 1974 Mar 28;21(4):315-21.

PMID:4135065

Abstract

摘要

相似文献

[Inherited translocation t(4q minus;18q plus) with unbalanced progeny of different types (author's transl)].[伴有不同类型不平衡子代的遗传性易位t(4号染色体长臂缺失；18号染色体长臂增加)(作者译)]

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引用本文的文献

Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies.伴有18号染色体长臂增加和18号染色体长臂缺失核型异常的选择性IgA缺乏症。

J Med Genet. 1980 Dec;17(6):453-6. doi: 10.1136/jmg.17.6.453.

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).由于父亲的平衡易位t(4q减;18q加)导致的4q部分三体和18q部分单体。

Humangenetik. 1974;25(3):227-33. doi: 10.1007/BF00281431.

Nonrandom distribution of exchange points in patients with structural rearrangements.结构重排患者交换点的非随机分布。

Am J Hum Genet. 1976 Jan;28(1):31-41.

Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation.由于母亲发生4/21易位，4号染色体长臂32区三体导致4号染色体长臂末端重复。

J Med Genet. 1975 Dec;12(4):425-7. doi: 10.1136/jmg.12.4.425.

Translocation +(7p+; Bq-) associated with recurrent abortion.与复发性流产相关的易位 +(7p+; Bq-)

Humangenetik. 1975 May 26;28(1):83-6. doi: 10.1007/BF00272488.

[Phenotypic variation in partial trisomy 4q (author's transl)].4q部分三体的表型变异（作者译）

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本文引用的文献

Mitotic and meiotic studies of a familial reciprocal translocation between autosomes 15 and 18 in man.人类15号与18号常染色体之间家族性相互易位的有丝分裂和减数分裂研究

Hereditas. 1967;58(3):303-24. doi: 10.1111/j.1601-5223.1967.tb02159.x.

Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome.

Ann Genet. 1971 Sep;14(3):187-92.

[On two familial cases of complex translocations].[关于两例复杂易位的家族性病例]

Ann Genet. 1965;8(1):21-30.

A modified method of culturing human amniotic fluid cells for prenatal detection of genetic disorders.

Humangenetik. 1972;14(4):333-4. doi: 10.1007/BF00290177.

[Complex chromosome changes bearing on the autosomes accompanying cranio-facial abnormalities and an umbilical hernia].

C R Acad Hebd Seances Acad Sci D. 1966 Jan 17;262(3):386-9.

[On pregnancies with a genetic high risk (technique, indications and results of genetic amniocentesis) (author's transl)].[关于具有遗传高风险的妊娠（遗传羊膜穿刺术的技术、适应症和结果）（作者译）]

Geburtshilfe Frauenheilkd. 1973 Aug;33(8):617-28.

Prenatal diagnosis of chromosome abnormalities.染色体异常的产前诊断

Acta Paediatr Scand. 1972 Jul;61(4):397-404. doi: 10.1111/j.1651-2227.1972.tb15854.x.

A rapid banding technique for routine use in human and comparative cytogenetics.一种用于人类和比较细胞遗传学常规检测的快速显带技术。

Humangenetik. 1972;15(4):349-53. doi: 10.1007/BF00281736.

Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.用盐酸阿的平荧光染色法鉴定唐氏综合征中的G组异常。

Humangenetik. 1971;12(1):67-73. doi: 10.1007/BF00291036.

[A case of a possible tandem-translocation C-13 in a boy with malformations].[一名患有畸形的男孩中可能存在串联易位C-13的病例]

Z Kinderheilkd. 1971;110(2):166-74.

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