Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association-Reference-Cited by-同舟云学术

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association

Published:1996-12-18 Issue:3 Volume:66 Page:347-355
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bahuau Michel,Flintoff Wayne,Assouline Brigitte,Lyonnet Stanislas,Le Merrer Martine,Prieur Marguerite,Guilloud-Bataille Michel,Feingold Nicole,Munnich Arnold,Vidaud Michel,Vidaud Dominique

Publisher

Wiley

Subject

Genetics (clinical)

Reference39 articles.

1. Neurofibromatosis with fully expressed Noonan syndrome

2. Noonan syndrome with café-au-lait spots and multiple lentigines syndrome are not linked to the neurofibromatosis type 1 locus

3. Noonan syndrome: The changing phenotype

4. Watson syndrome: is it a subtype of type 1 neurofibromatosis?

5. Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues.

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