Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

K M Cerosaletti; E Lange; H M Stringham; C M Weemaes; D Smeets; B Sölder; B H Belohradsky; A M Taylor; P Karnes; A Elliott

doi:10.1086/301927

Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

NobleID: NI0P01W23R54S18
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/DC8EED2E

Type:Journal Article

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Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.

NobleID: NI0P01W23R54S18
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/DC8EED2E

Type:Journal Article

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