Sequential G-banding FISH on human sperm chromosomes

No abstract is available for this paper.

• Publication year

  1997

• Venue

  Chromosome Research

• Publication date

  1997-11-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1023/A:1018464929628PMID 9421262
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1983cited by this paper
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  1982cited by this paper
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  1966cited by this paper
• Direct Analysis of

  year unknowninfluential reference

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  2016influential citation
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  2014cites this paper
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