Limiting subsequent mutagenic events in carriers of hereditary tumor genes.

Por Jackson, C E
Publicado em 1992

Three Cases of Gastric Carcinoma Presenting Unusual Features

Por Jackson, C. E. S.
Publicado em 1923

ACUTE INTESTINAL OBSTRUCTION DUE TO PREGNANCY IN A BICORNUATE UTERUS

Por Jackson, C. E. S.
Publicado em 1920

Amish albinism: a distinctive autosomal recessive phenotype.

Por Nance, W E, Jackson, C E, Witkop, C J
Publicado em 1970

Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

Por Babu, V R, Van Dyke, D L, Jackson, C E
Publicado em 1984

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneity.

Por Heath, H, Jackson, C E, Otterud, B, Leppert, M F
Publicado em 1993

Characterization of calcium-dependent membrane binding proteins of brain cortex.

Por Rhoads, A R, Lulla, M, Moore, P B, Jackson, C E
Publicado em 1985

Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic...

Por Jin, W D, Jackson, C E, Desnick, R J, Schuchman, E H
Publicado em 1992

The two-mutational-event theory in medullary thyroid cancer.

Por Jackson, C E, Block, M A, Greenawald, K A, Tashjian, A H
Publicado em 1979

The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.

Por Carson, N L, Wu, J S, Jackson, C E, Kidd, K K, Simpson, N E
Publicado em 1990

Consanguinity and blood group distribution in an Amish Isolate.

Por Jackson, C E, Symon, W E, Pruden, E L, Kaehr, I M, Mann, J D
Publicado em 1968

DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.

Por Pratt, V M, Jackson, C E, Wallace, D C, Gurley, D S, Feit, A, Feldman, G L
Publicado em 1997

The physicochemical properties of hair in the BIDS syndrome.

Por Baden, H P, Jackson, C E, Weiss, L, Jimbow, K, Lee, L, Kubilus, J, Gold, R J
Publicado em 1976

Parent-of-origin effects in multiple endocrine neoplasia type 2B.

Por Carlson, K. M., Bracamontes, J., Jackson, C. E., Clark, R., Lacroix, A., Wells, S. A., Goodfellow, P. J.
Publicado em 1994

Phenylketonuria heterozygote detection in families with affected children.

Por Paul, T D, Brandt, I K, Elsas, L J, Jackson, C E, Mamunes, P, Nance, C S, Nance, W E
Publicado em 1978

Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.

Por Carlson, K M, Dou, S, Chi, D, Scavarda, N, Toshima, K, Jackson, C E, Wells, S A, Goodfellow, P J, Donis-Keller, H
Publicado em 1994

Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinism.

Por Giebel, L B, Tripathi, R K, Strunk, K M, Hanifin, J M, Jackson, C E, King, R A, Spritz, R A
Publicado em 1991

Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q.

Por Hobbs, M R, Pole, A R, Pidwirny, G N, Rosen, I B, Zarbo, R J, Coon, H, Heath, H, Leppert, M, Jackson, C E
Publicado em 1999

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.

Por Berg, J N, Gallione, C J, Stenzel, T T, Johnson, D W, Allen, W P, Schwartz, C E, Jackson, C E, Porteous, M E, Marchuk, D A
Publicado em 1997

Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31.

Por Feit, H, Silbergleit, A, Schneider, L B, Gutierrez, J A, Fitoussi, R P, Réyès, C, Rouleau, G A, Brais, B, Jackson, C E, Beckmann, J S, Seboun, E
Publicado em 1998