Authors: KORGE BP HEALY E TRAUPE H PUNTER C MAUCH C HAMM H BIRCHMACHIN MA BELGAID CE STEPHENSON AM HOLMES SC DARLINGTON S MESSENGER AG REES JL MUNRO CS

Citation: Bp. Korge et al., MONILETHRIX IS CAUSED BY MUTATION IN THE HELIX TERMINATION PEPTIDE OFHUMAN TYPE-II HAIR KERATIN HHB6 IN 3 FAMILIES, Journal of investigative dermatology, 109(3), 1997, pp. 409-409

Authors: ISHIDAYAMAMOTO A KORGE BP PUENTER C DOPPINGHEPENSTAL T HOHL D IIZUKA H STEPHENSON AM EADY RAJ MUNRO CS

Citation: A. Ishidayamamoto et al., ABNORMAL KERATINIZATION AND LORICRIN MUTATION IN VOHWINKELS-SYNDROME (VS) WITH ICHTHYOSIS, Journal of investigative dermatology, 108(4), 1997, pp. 642-642

Authors: BIRCHMACHIN MA HEALY E TURNER R HALDANE F BELGAID CE DARLINGTON S STEPHENSON AM MUNRO C MESSENGER AG REES JL

Citation: Ma. Birchmachin et al., MAPPING OF MONILETHRIX TO THE TYPE-II KERATIN GENE-CLUSTER AT CHROMOSOME 12Q13 IN 3 NEW FAMILIES, INCLUDING ONE WITH VARIABLE EXPRESSIVITY, British journal of dermatology, 137(3), 1997, pp. 339-343

Authors: HEALY E HOLMES SC BELGAID CE STEPHENSON AM MCLEAN WHI REES JL MUNRO CS

Citation: E. Healy et al., A GENE FOR MONILETHRIX IS CLOSELY LINKED TO THE TYPE-II KERATIN GENE-CLUSTER AT 12Q13, Human molecular genetics, 4(12), 1995, pp. 2399-2402

Authors: INGLEHEARN CF CARTER SA KEEN TJ LINDSEY J STEPHENSON AM BASHIR R ALMAGHTHEH M MOORE AT JAY M BIRD AC BHATTACHARYA SS

Citation: Cf. Inglehearn et al., A NEW LOCUS FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA ON CHROMOSOME-7P, Nature genetics, 4(1), 1993, pp. 51-53