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Karyotype, meiosis and spermatogenesis in a sample of men attending an infertility clinic.

作者信息

Kjessler B

出版信息

Monogr Hum Genet. 1966;2:1-93.

PMID:6015462
Abstract
摘要

相似文献

1
Karyotype, meiosis and spermatogenesis in a sample of men attending an infertility clinic.
Monogr Hum Genet. 1966;2:1-93.
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引用本文的文献

1
Karyotypic abnormalities and Y chromosome microdeletions: How do these impact in vitro fertilization outcomes, and how common are they in the modern in vitro fertilization practice?染色体核型异常与Y染色体微缺失：它们如何影响体外受精结果，在现代体外受精实践中又有多常见？
F S Rep. 2021 Jun 11;2(3):300-307. doi: 10.1016/j.xfre.2021.06.001. eCollection 2021 Sep.
2
Very low sperm count affects the result of intracytoplasmic sperm injection.极低的精子计数会影响卵胞浆内单精子注射的结果。
J Assist Reprod Genet. 2000 Sep;17(8):431-6. doi: 10.1023/a:1009413201849.
3
Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XXY male.
通过三色荧光原位杂交技术在一名46,XY/47,XXY男性中检测到超单倍体24,XY精子发生率增加。
Hum Genet. 1996 Feb;97(2):171-5. doi: 10.1007/BF02265260.
4
Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient.
Hum Genet. 1994 Jan;93(1):32-4. doi: 10.1007/BF00218909.
5
Synaptonemal complex studies in a mosaic 46,XY/47,XXY male.
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6
Chromosome studies in 496 infertile males with a sperm count below 10 million/ml.
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7
[A case with balanced (14p+; 15p minus)-translocation].[一例平衡型（14号染色体短臂增加；15号染色体短臂缺失）易位病例]
Humangenetik. 1970;8(4):312-20. doi: 10.1007/BF00280330.
8
Nucleoli and chromosomes: their relationships during the meiotic prophase of the human fetal oocyte.核仁与染色体：人类胎儿卵母细胞减数分裂前期它们之间的关系
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Uveal coloboma and true Klinefelter syndrome.葡萄膜缺损和真性克兰费尔特综合征。
J Med Genet. 1970 Sep;7(3):213-23. doi: 10.1136/jmg.7.3.213.
10
[The nosologic place of the XO-XY mosaicism].[XO-XY 嵌合体的疾病分类位置]
Arch Gynakol. 1968;206(4):369-410. doi: 10.1007/BF00668069.