Bibliotecas PUC-SP - Busca Integrada

Polydactyly: a study of a five generation Indian family.

بواسطة Radhakrishna, U, Multani, A S, Solanki, J V, Shah, V C, Chinoy, N J
منشور في 1993

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

بواسطة Radhakrishna, U, Blouin, J L, Mehenni, H, Patel, U C, Patel, M N, Solanki, J V, Antonarakis, S E
منشور في 1997

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

بواسطة Mehenni, H, Blouin, J L, Radhakrishna, U, Bhardwaj, S S, Bhardwaj, K, Dixit, V B, Richards, K F, Bermejo-Fenoll, A, Leal, A S, Raval, R C, Antonarakis, S E
منشور في 1997

The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position...

بواسطة Radhakrishna, U, Bornholdt, D, Scott, H S, Patel, U C, Rossier, C, Engel, H, Bottani, A, Chandal, D, Blouin, J L, Solanki, J V, Grzeschik, K H, Antonarakis, S E
منشور في 1999

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

بواسطة Ben-Yosef, T., Wattenhofer, M., Riazuddin, S., Ahmed, Z., Scott, H., Kudoh, J., Shibuya, K., Antonarakis, S., Bonne-Tamir, B., Radhakrishna, U., Naz, S., Ahmed, Z., Riazuddin, S., Pandya, A., Nance, W., Wilcox, E., Friedman, T., Morell, R.
منشور في 2001