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November 1, 1998Human Reproduction

A familial case of X chromosome deletion ascertained by cytogenetic screening of women with premature ovarian failure

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Authors

RDRina M. DavisonMiddlesex HospitalCQClaire R. QuilterUniversity of CambridgeJWJames L. WebbQuantumWise (Denmark)

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Davison et al. (1998) studied this question.

synapsesocial.com/papers/6a75b9aa72aedb66d66a3c6fhttps://doi.org/10.1093/humrep/13.11.3039
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1FRAXA premutation associated with premature ovarian failure1996 · 64 citations
  2. 2Familial Premature Ovarian Failure Due to an Interstitial Deletion of the Long Arm of the X Chromosome1987 · 204 citations
  3. 3Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.1988 · 1,339 citations
  4. 4Obstetrical and gynecological complications in fragile X carriers: A multicenter study1994 · 207 citations
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