PHYSICAL METALLURGY OF ENGINEERING MATERIALS.

Por PETTY E R.
Publicado em 1968.

MARTENSITE;FUNDAMENTALS AND TECHNOLOGY.

Por PETTY E R.
Publicado em C1970

PHYSICAL METALLURGY OF ENGINEERING MATERIALS.

Por PETTY E R.
Publicado em 1968.

Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1

Por Hedera, P, Toriello, H, Petty, E
Publicado em 2002

Characterisation and genetic mapping of a new X linked deafness syndrome

Por Martin, D., Probst, F., Camper, S., Petty, E.
Publicado em 2000

Ornithine transcarbamylase polymorphism detected by PCR introduction of Dral site

Por Petty, E.M., Carstens, R., Bale, A.E.
Publicado em 1991

Questioning the need for anonymous genetic counseling and testing.

Por Uhlmann, W. R., Ginsburg, D., Gelehrter, T. D., Nicholson, J., Petty, E. M.
Publicado em 1996

Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.

Por Petty, E. M., Green, J. S., Marx, S. J., Taggart, R. T., Farid, N., Bale, A. E.
Publicado em 1994

Understandings of Basic Genetics in the United States: Results from a National Survey of Black and White Men and Women

Por Christensen, K.D., Jayaratne, T.E., Roberts, J.S., Kardia, S.L.R., Petty, E.M.
Publicado em 2010

PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.

Por Rosenberg, C L, Wong, E, Petty, E M, Bale, A E, Tsujimoto, Y, Harris, N L, Arnold, A
Publicado em 1991

Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).

Por Petty, E M, Gibson, L H, Fountain, J W, Bolognia, J L, Yang-Feng, T L, Housman, D E, Bale, A E
Publicado em 1993

Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.

Por Smith, L T, Wertelecki, W, Milstone, L M, Petty, E M, Seashore, M R, Braverman, I M, Jenkins, T G, Byers, P H
Publicado em 1992

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.

Por Colige, A, Sieron, A L, Li, S W, Schwarze, U, Petty, E, Wertelecki, W, Wilcox, W, Krakow, D, Cohn, D H, Reardon, W, Byers, P H, Lapière, C M, Prockop, D J, Nusgens, B V
Publicado em 1999