Refined Mapping of Naegeli–Franceschetti– Jadassohn Syndrome to a 6 cM Interval on Chromosome 17q11.2-q21 and Investigation of Candidate Genes-Reference-Cited by-同舟云学术

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Refined Mapping of Naegeli–Franceschetti– Jadassohn Syndrome to a 6 cM Interval on Chromosome 17q11.2-q21 and Investigation of Candidate Genes

Published:2002-09 Issue:3 Volume:119 Page:692-698
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Sprecher Eli,Uitto Jouni,Richard Gabriele,Itin Peter,Whittock Neil V.,McGrath John A.,Meyer Rudolph,DiGiovanna John J.,Bale Sherri J.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference30 articles.

1. Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21;Aita;Genomics,1999

2. Cytokeratin-positive malignant tumors with reticulum cell morphology: a subtype of fibroblastic reticulum cell neoplasm?;Chan;Am J Surg Pathol,2000

3. Cytokeratin-immunoreactive cells of human lymph nodes and spleen in normal and pathological conditions. An immunocytochemical study;Doglioni;Virchows Arch Pathol Anat Histopathol,1990

4. A propos de ‘l’incontinentia pigmenti', delimitation de deux syndromes differents figurant sous le meme terme;Franceschetti;Dermatologica,1954

5. The Nageli–Franceschetti–Jadassohn syndrome: a hereditary ectodermal defect leading to colloid-amyloid formation in the dermis;Frenk;Dermatology,1993

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