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