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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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J Celli

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Human Mutation|April 27, 2011

LOVD v.2.0: the next generation in gene variant databasesIvo F A C Fokkema, Peter E M Taschner, Gerard C P Schaafsma, et al.

Revista De La Facultad De Ciencias Medicas (Cordoba, Argentina)|January 1, 1997

[Clinical and epidemiologic characteristics of acute diarrhea in adults at a hospital from Cordoba city]H Polo Friz, S Toloza, H Acosta, et al.

Nature Genetics|August 10, 2000

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.

American Journal of Human Genetics|March 21, 2000

Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.

Cell|October 27, 1999

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.

American Journal of Human Genetics|July 20, 2001

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.

Pageof 2

Search research articles

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

Human Mutation|April 27, 2011

LOVD v.2.0: the next generation in gene variant databasesIvo F A C Fokkema, Peter E M Taschner, Gerard C P Schaafsma, et al.

Revista De La Facultad De Ciencias Medicas (Cordoba, Argentina)|January 1, 1997

[Clinical and epidemiologic characteristics of acute diarrhea in adults at a hospital from Cordoba city]H Polo Friz, S Toloza, H Acosta, et al.

Nature Genetics|August 10, 2000

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.

American Journal of Human Genetics|March 21, 2000

Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.

Cell|October 27, 1999

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndromeJ Celli, P Duijf, B C Hamel, et al.

American Journal of Human Genetics|July 20, 2001

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlationH van Bokhoven, B C Hamel, M Bamshad, et al.

Pageof 2