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A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defects

Published in: British Journal of Dermatology

Date of publication: November 1, 1994

Language: English

Main subject: X-linked ichthyosis

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Cites articles 9

Date

Title

Authors

March 1, 1979

Congenital anosmia: detection thresholds for seven odorant classes in hypogonadal and eugonadal patients
January 1, 1982

Review: placental sulphatase deficiency,Review: Placental sulphatase deficiency
October 1, 1982

Syndrome of anosmia with hypogonadotropic hypogonadism (Kallmann syndrome): clinical and laboratory studies in 23 cases
March 1, 1983

Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism
September 1, 1988

Chondrodysplasia punctata with X;Y translocation
December 1, 1989

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome
July 1, 1990

An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature
October 10, 1991

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
October 18, 1991

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

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