Eng C - Search Results

1

A novel polymorphism in the coding sequence of the human RET proto-oncogene.

Edery P, Attié T, Mulligan LM, Pelet A, Eng C, Ponder BA, Munnich A, Lyonnet S. Edery P, et al. Among authors: eng c. Hum Genet. 1994 Nov;94(5):579-80. doi: 10.1007/BF00211034. Hum Genet. 1994. PMID: 7959702

2

Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.

Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S. Bidaud C, et al. Among authors: eng c. Eur J Hum Genet. 1997 Jul-Aug;5(4):247-51. Eur J Hum Genet. 1997. PMID: 9359047

3

Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.

Attié T, Pelet A, Edery P, Eng C, Mulligan LM, Amiel J, Boutrand L, Beldjord C, Nihoul-Fékété C, Munnich A, et al. Attié T, et al. Among authors: eng c. Hum Mol Genet. 1995 Aug;4(8):1381-6. doi: 10.1093/hmg/4.8.1381. Hum Mol Genet. 1995. PMID: 7581377

4

Haplotype analysis of MEN 2 mutations.

Gardner E, Mulligan LM, Eng C, Healey CS, Kwok JB, Ponder MA, Ponder BA. Gardner E, et al. Among authors: eng c. Hum Mol Genet. 1994 Oct;3(10):1771-4. doi: 10.1093/hmg/3.10.1771. Hum Mol Genet. 1994. PMID: 7849700

5

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

Mulligan LM, Eng C, Attié T, Lyonnet S, Marsh DJ, Hyland VJ, Robinson BG, Frilling A, Verellen-Dumoulin C, Safar A, et al. Mulligan LM, et al. Among authors: eng c. Hum Mol Genet. 1994 Dec;3(12):2163-7. doi: 10.1093/hmg/3.12.2163. Hum Mol Genet. 1994. PMID: 7881414

6

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.

Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Scheumann GF, Jackson CE, Tunnacliffe A, et al. Eng C, et al. Hum Mol Genet. 1994 Feb;3(2):237-41. doi: 10.1093/hmg/3.2.237. Hum Mol Genet. 1994. PMID: 7911697

7

A de novo mutation of the RET proto-oncogene in a patient with MEN 2A.

Mulligan LM, Eng C, Healey CS, Ponder MA, Feldman GL, Li P, Jackson CE, Ponder BA. Mulligan LM, et al. Among authors: eng c. Hum Mol Genet. 1994 Jun;3(6):1007-8. doi: 10.1093/hmg/3.6.1007. Hum Mol Genet. 1994. PMID: 7951212 No abstract available.

8

A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung's disease.

Attie T, Pelet A, Sarda P, Eng C, Edery P, Mulligan LM, Ponder BA, Munnich A, Lyonnet S. Attie T, et al. Among authors: eng c. Hum Mol Genet. 1994 Aug;3(8):1439-40. doi: 10.1093/hmg/3.8.1439. Hum Mol Genet. 1994. PMID: 7987334 No abstract available.

9

Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.

Salomon R, Attié T, Pelet A, Bidaud C, Eng C, Amiel J, Sarnacki S, Goulet O, Ricour C, Nihoul-Fékété C, Munnich A, Lyonnet S. Salomon R, et al. Among authors: eng c. Nat Genet. 1996 Nov;14(3):345-7. doi: 10.1038/ng1196-345. Nat Genet. 1996. PMID: 8896569

10

De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.

Ivanchuk SM, Myers SM, Eng C, Mulligan LM. Ivanchuk SM, et al. Among authors: eng c. Hum Mol Genet. 1996 Dec;5(12):2023-6. doi: 10.1093/hmg/5.12.2023. Hum Mol Genet. 1996. PMID: 8968758

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,912 results

Search Page

Filters