Stephen W. Scherer

发表

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.

S. Scherer, L. Tsui, J. Rommens, 1996, Human molecular genetics.

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.

S. Scherer, L. Tsui, M. Muenke, 1997, Human molecular genetics.

Involvement of the HLXB9 homeobox gene in Currarino syndrome.

S. Scherer, L. Tsui, V. Jasonni, 2000, American journal of human genetics.

Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5.

S Schwartz, W Miller, S W Scherer, 2001, Nucleic acids research.

Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

S. Scherer, M. Patton, R. Pagon, 1994, American journal of human genetics.

Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition.

S. Scherer, N. Royle, H. Varley, 2000, American journal of human genetics.

Regional localization of 725 human chromosome 7-specific yeast artificial chromosome clones.

S. Scherer, H. Heng, L. Tsui, 1994, Genomics.

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.

J. Rommens, M. Crackower, P. Poorkaj, 1996, Human molecular genetics.

Holoprosencephaly and cleidocranial dysplasia in a patient due to two position‐effect mutations: case report and review of the literature

J. Herbrick, I. Teshima, J. Siegel‐Bartelt, 2005, Clinical genetics.

Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia.

S. Scherer, L. Tsui, D. Oscier, 1996, Blood.

Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET.

S. Scherer, L. Tsui, I. Andrulis, 1996, Oncogene.