Literature DB >> 1132157

Incontinentia pigmenti.

T Iancu, L Komlos, F Shabtay, E Elian, L Halbrecht, J A Böök.   

Abstract

Four new cases of incontinentia pigmenti are presented, including chromosome studies of one family. An increased number of chromosome breakages was found in the blood of affected as well as unaffected members of this family.

Entities:  

Mesh：

Year:  1975        PMID： 1132157     DOI： 10.1111/j.1399-0004.1975.tb00305.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  8 in total

1.  [Neuropathological study of incontinentia pigmenti. Anatomical case report (author's transl)].

Authors:  J J Hauw; G Perié; J Bonnette; R Escourolle
Journal:  Acta Neuropathol       Date:  1977-05-16       Impact factor: 17.088

2.  Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.

Authors:  A Sefiani; D Sinnett; L Abel; S Szpiro-Tapia; S Heuertz; I Craig; N Fraser; T A Kruse; M Frydman; M O Peter
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

Review 3.  Incontinentia pigmenti (Bloch-Sulzberger syndrome).

Authors:  S J Landy; D Donnai
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

4.  Asymmetry and skin pigmentary anomalies in chromosome mosaicism.

Authors:  C G Woods; A Bankier; J Curry; L J Sheffield; S F Slaney; K Smith; L Voullaire; D Wellesley
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

5.  Studies of a family with incontinentia pigmenti variably expressed in both sexes.

Authors:  T W Kurczynski; J S Berns; W E Johnson
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

Review 6.  Lyonization and the lines of Blaschko.

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

7.  Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.

Authors:  A Sefiani; R M'rad; L Simard; A Vincent; C Julier; L Holvoet-Vermaut; S Heuertz; N Dahl; J F Stalder; M O Peter
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

8.  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
  8 in total

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