Genetic counselling in hypomelanosis of Ito: case report and review-Reference-Cited by-同舟云学术

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Genetic counselling in hypomelanosis of Ito: case report and review

Published:2008-06-28 Issue:2 Volume:34 Page:109-115
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Moss Celia,Burn John

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb02845.x/fullpdf

Reference41 articles.

1. Single maxillary central incisor and coloboma in hypomelanosis of Ito;Bartholemew;Clin. Genet.,1987

2. Eigentumlicher, bisher nicht beschriebene Pigmentaffektion (Incontinentia pigmenti);Bloch;Schweiz. Med. Wochenschr.,1926

3. Dental dysplasia in incontinentia pigmenti achromians (Ito): an unusual form;Browne;Br. Dent. J.,1976

4. Hypomelanose de Ito. Revue de la litterature à propos de 3 cas;Cambazard;Ann. Dermatol. Venereol.,1986

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hypomelanosis of Ito;Neurocutaneous Syndromes;2015

2. Hypomélanose de Ito et mosaïcismes pigmentaires;Manifestations dermatologiques des maladies d’organes;2012

3. Hypomelanosis of Ito;Atlas of Genetic Diagnosis and Counseling;2012

4. Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature;Neurological Sciences;2009-11-10

5. Cytogenetic and dermatoglyphic findings in a familial case of hypomelanosis of Ito (incontinentia pigmenti achromians);Clinical Genetics;2008-06-28

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