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List of works by Thomas King

Deletion mapping by immunoselection against the H-Y histocompatibility antigen further resolves the Sxra region of the mouse Y chromosome and reveals complexity of the Hya locus.

scientific article published on November 1994

Mapping anti-müllerian hormone (Amh) and related sequences in the mouse: identification of a new region of homology between MMU10 and HSA19p

scientific article published on 01 October 1991

Meiotic mapping of murine chromosome 17: The string of loci around l(17)-2Pas ⬇️

scientific article published on January 1, 1991

Molecular genetic mapping of the mouse male sterility and histoincompatibility (mshi) mutation on proximal chromosome 10

scientific article published on 01 January 1997

Mouse male sterility and histoincompatibility (mshi) maps between the D10Mit51/168/212 cluster and D10Mit213

scientific article published on 01 May 1999

Pleiotropic action of the murine quaking locus: structure of the qkv allele.

scientific article published in January 1991

Shorn (shn): a new mutation causing hypotrichosis in the Norway rat

scientific article published on 01 May 1998

The H-mshi antigen is conserved among standard BALB/cBy, C57BL/6J, and wild-derived CAST/Ei and SPRET/Ei inbred strains of mice

scientific article published on 01 July 1999

The juvenile alopecia mutation (jal) maps to mouse Chromosome 2, and is an allele of GATA binding protein 3 (Gata3).

scientific article

The mouse Y* chromosome involves a complex rearrangement, including interstitial positioning of the pseudoautosomal region.

scientific article published on January 1991

The mouse frizzy mutation (fr) maps between D7Csu5 and D7Mit165

scientific article published on 31 December 2007

The mouse wellhaarig (we) mutations result from defects in epidermal-type transglutaminase 3 (Tgm3)

scientific article

The rat shorn mutation (shn) maps between D7Got143 and D7Rat94

scientific article published on 01 August 2002

The retarded hair growth (rhg) mutation in mice is an allele of ornithine aminotransferase (Oat).

scientific article

The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g ⬇️

scientific article published on May 9, 2013

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