Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 2
1996 1
1997 2
1998 3
2021 0
Text availability
Article attribute
Article type
Publication date

Search Results

9 results
Results by year
Filters applied: . Clear all
Page 1
Endothelin receptor-mediated signaling in hirschsprung disease.
Chakravarti A. Chakravarti A. Hum Mol Genet. 1996 Mar;5(3):303-7. Hum Mol Genet. 1996. PMID: 8852653 Review. No abstract available.
Does phaster mean better?
Angrist M. Angrist M. Clin Chem. 1997 Mar;43(3):424-6. Clin Chem. 1997. PMID: 9068584 No abstract available.
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
Angrist M, Kauffman E, Slaugenhaupt SA, Matise TC, Puffenberger EG, Washington SS, Lipson A, Cass DT, Reyna T, Weeks DE, et al. Angrist M, et al. Nat Genet. 1993 Aug;4(4):351-6. doi: 10.1038/ng0893-351. Nat Genet. 1993. PMID: 8401581
Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.
Angrist M, Jing S, Bolk S, Bentley K, Nallasamy S, Halushka M, Fox GM, Chakravarti A. Angrist M, et al. Genomics. 1998 Mar 15;48(3):354-62. doi: 10.1006/geno.1997.5191. Genomics. 1998. PMID: 9545641
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.
Puffenberger EG, Kauffman ER, Bolk S, Matise TC, Washington SS, Angrist M, Weissenbach J, Garver KL, Mascari M, Ladda R, et al. Puffenberger EG, et al. Hum Mol Genet. 1994 Aug;3(8):1217-25. doi: 10.1093/hmg/3.8.1217. Hum Mol Genet. 1994. PMID: 7987295
Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.
Angrist M, Bolk S, Bentley K, Nallasamy S, Halushka MK, Chakravarti A. Angrist M, et al. Oncogene. 1998 Dec 10;17(23):3065-70. doi: 10.1038/sj.onc.1202226. Oncogene. 1998. PMID: 9881709
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Carrasquillo MM, Zlotogora J, Barges S, Chakravarti A. Carrasquillo MM, et al. Hum Mol Genet. 1997 Nov;6(12):2163-72. doi: 10.1093/hmg/6.12.2163. Hum Mol Genet. 1997. PMID: 9328482
A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease.
Puffenberger EG, Hosoda K, Washington SS, Nakao K, deWit D, Yanagisawa M, Chakravart A. Puffenberger EG, et al. Cell. 1994 Dec 30;79(7):1257-66. doi: 10.1016/0092-8674(94)90016-7. Cell. 1994. PMID: 8001158
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.
Shaw SH, Carrasquillo MM, Kashuk C, Puffenberger EG, Chakravarti A. Shaw SH, et al. Genome Res. 1998 Feb;8(2):111-23. doi: 10.1101/gr.8.2.111. Genome Res. 1998. PMID: 9477339 Free article.