Exclusion of retinoic acid receptor and a cartilage matrix protein in non-syndromic CL(P) families.

Por Stein, J D, Hecht, J T, Blanton, S H
Publicado em 1995

Examinations of Methylenetetrahydrofolate Reductase C677T and A1298C Mutations—and In Utero Viability

Por Volcik, K. A., Blanton, S. H., Northrup, H.
Publicado em 2001

Association of ABCA4 and MAFB with nonsyndromic cleft lip with or without cleft palate

Por Yuan, Qiuping, Blanton, Susan H., Hecht, Jacqueline T.
Publicado em 2011

Van der Woude syndrome and nonsyndromic cleft lip and palate.

Por Hecht, J T, Wang, Y, Blanton, S H, Daiger, S P
Publicado em 1992

Dinucleotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT)

Por Sadler, L.A., Blanton, S.H., Daiger, S.P.
Publicado em 1991

Evaluation of candidate genes for familial brachydactyly.

Por Mastrobattista, J M, Dollé, P, Blanton, S H, Northrup, H
Publicado em 1995

Report of a critical recombination further narrowing the TSC1 region.

Por Au, K S, Murrell, J, Buckler, A, Blanton, S H, Northrup, H
Publicado em 1996

Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A.

Por Hecht, J T, Wang, Y, Connor, B, Blanton, S H, Daiger, S P
Publicado em 1993

Next-Generation Sequencing in Genetic Hearing Loss

Por Yan, Denise, Tekin, Mustafa, Blanton, Susan H., Liu, Xue Zhong
Publicado em 2013

Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly

Por Kumar, Arun, Girimaji, Satish C., Duvvari, Mahesh R., Blanton, Susan H.
Publicado em 2009

Cleft lip and palate: no evidence of linkage to transforming growth factor alpha.

Por Hecht, J T, Wang, Y P, Blanton, S H, Michels, V V, Daiger, S P
Publicado em 1991

Reply to Farrall et al

Por Hecht, Jacqueline T., Wang, Yaping, Blanton, Susan H., Michels, Virginia V., Daiger, Stephen P.
Publicado em 1993

A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL11) locus

Por Cottingham, A.W., Blanton, S.H., Retief, A.E., Warnich, L., Daiger, S.P.
Publicado em 1991

Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8.

Por Hecht, J T, Hogue, D, Strong, L C, Hansen, M F, Blanton, S H, Wagner, M
Publicado em 1995

Family-based study shows heterogeneity of a susceptibility locus on chromosome 8q24 for nonsyndromic cleft lip and palate

Por Blanton, Susan H., Burt, Amber, Stal, Samuel, Mulliken, John B., Garcia, Elizabeth, Hecht, Jacqueline T.
Publicado em 2010

Ethnic heterogeneity of IRF6 AP-2α binding site promoter SNP association with nonsyndromic cleft lip and palate

Por Blanton, Susan H., Burt, Amber, Garcia, Elizabeth, Mulliken, John B., Stal, Samuel, Hecht, Jacqueline T.
Publicado em 2010

Follow-Up Association Study of Linkage Regions Reveals Multiple Candidate Genes for Carotid Plaque in Dominicans

Por Dong, Chuanhui, Beecham, Ashley, Wang, Liyong, Blanton, Susan H., Rundek, Tatjana, Sacco, Ralph L.
Publicado em 2012

Sequencing of Candidate Genes in Dominican Families Implicates Both Rare Exonic and Common Non-Exonic Variants for Carotid Intima-Media Thickness at Bifurcation

Por Wang, Liyong, Beecham, Ashley, Dueker, Nicole, Blanton, Susan H., Rundek, Tatjana, Sacco, Ralph L.
Publicado no Hum Genet (2015)

Further Evidence Suggesting a Role for Variation in ARHGAP29 in Nonsyndromic Cleft Lip/Palate

Por Letra, A., Maili, L., Mulliken, J.B., Buchanan, E., Blanton, S.H., Hecht, J.T.
Publicado no Birth Defects Res A Clin Mol Teratol (2014)

Sickle Cell Trait and Renal Function in Hispanics in the United States: The Northern Manhattan Study

Por Dueker, Nicole D., Della-Morte, David, Rundek, Tatjana, Sacco, Ralph L., Blanton, Susan H.
Publicado no Ethn Dis (2017)