Literature DB >> 15392890

Follicular atrophoderma and pseudopelade associated with chondrodystrophia calcificans congenita.

H O CURTH.   

Abstract

Entities:  

Keywords:  ACHONDROPLASIA; ALOPECIA; SKIN

Mesh：

Year:  1949        PMID： 15392890     DOI： 10.1038/jid.1949.95

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  7 in total

1.  Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation.

Authors:  H Traupe; D Müller; D Atherton; D C Kalter; F P Cremers; B A van Oost; H H Ropers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  [Incontinentia pigmenti syndrome].

Authors:  P WODNIANSKY
Journal:  Arch Klin Exp Dermatol       Date:  1955

3.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

Review 4.  Lyonization and the lines of Blaschko.

Authors:  R Happle
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

5.  X-linked dominant chondrodysplasia punctata. Review of literature and report of a case.

Authors:  R Happle
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

6.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Ocular changes in the Bloch-Sulzberger syndrome (Incontinentia pigmenti)

Authors:  J G SCOTT; A I FRIEDMANN; M CHITTERS; W J PEPLER
Journal:  Br J Ophthalmol       Date:  1955-05       Impact factor: 4.638
  7 in total

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