The genetics of Alzheimer disease--a teasing problem.

Por Haines, J L
Publicado em 1991

Dinucleotide repeat polymorphism at the debrisoquine 4-hydroxylase (CYP2D) locus

Por Trofatter, J.A., Gusella, J.F., Haines, J.L.
Publicado em 1991

LIPIN: an interactive data entry and management program for LIPED.

Por Trofatter, J A, Haines, J L, Conneally, P M
Publicado em 1986

Fine mapping of the GLC1K juvenile primary open-angle glaucoma locus and exclusion of candidate genes

Por Sud, A., Del Bono, E.A., Haines, J.L., Wiggs, J.L.
Publicado em 2008

An index marker map of chromosome 9 provides strong evidence for positive interference.

Por Kwiatkowski, D J, Dib, C, Slaugenhaupt, S A, Povey, S, Gusella, J F, Haines, J L
Publicado em 1993

Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.

Por Ionasescu, V V, Trofatter, J, Haines, J L, Summers, A M, Ionasescu, R, Searby, C
Publicado em 1991

Exclusion of chromosome 1q21-q31 from linkage to three pedigrees affected by the pigment-dispersion syndrome.

Por Paglinauan, C, Haines, J L, Del Bono, E A, Schuman, J, Stawski, S, Wiggs, J L
Publicado em 1995

The distinction between juvenile and adult-onset primary open-angle glaucoma.

Por Wiggs, J. L., Damji, K. F., Haines, J. L., Pericak-Vance, M. A., Allingham, R. R.
Publicado em 1996

Linkage localization of X-linked Charcot-Marie-Tooth disease.

Por Bergoffen, J, Trofatter, J, Pericak-Vance, M A, Haines, J L, Chance, P F, Fischbeck, K H
Publicado em 1993

A genetic linkage map of human chromosome 21: analysis of recombination as a function of sex and age.

Por Tanzi, R E, Watkins, P C, Stewart, G D, Wexler, N S, Gusella, J F, Haines, J L
Publicado em 1992

A Genomewide Scan Identifies Novel Early-Onset Primary Open-Angle Glaucoma Loci on 9q22 and 20p12

Por Wiggs, J. L., Lynch, S., Ynagi, G., Maselli, M., Auguste, J., Del Bono, E. A., Olson, L. M., Haines, J. L.
Publicado em 2004

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Por Rouleau, G A, Seizinger, B R, Wertelecki, W, Haines, J L, Superneau, D W, Martuza, R L, Gusella, J F
Publicado em 1990

DNA linkage analysis of X chromosome-linked chronic granulomatous disease.

Por Baehner, R L, Kunkel, L M, Monaco, A P, Haines, J L, Conneally, P M, Palmer, C, Heerema, N, Orkin, S H
Publicado em 1986

A second locus for Rieger syndrome maps to chromosome 13q14.

Por Phillips, J. C., del Bono, E. A., Haines, J. L., Pralea, A. M., Cohen, J. S., Greff, L. J., Wiggs, J. L.
Publicado em 1996

Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1.

Por Lerner, T. J., Boustany, R. M., MacCormack, K., Gleitsman, J., Schlumpf, K., Breakefield, X. O., Gusella, J. F., Haines, J. L.
Publicado em 1994

A Genome-wide Scan in an Amish Pedigree with Parkinsonism

Por LEE, S. L., MURDOCK, D. G., MCCAULEY, J. L., BRADFORD, Y., CRUNK, A., MCFARLAND, L., JIANG, L., WANG, T., SCHNETZ-BOUTAUD, N., HAINES, J. L.
Publicado em 2008

Comparative mapping of DNA markers from the familial Alzheimer disease and Down syndrome regions of human chromosome 21 to mouse chromosomes 16 and 17.

Por Cheng, S V, Nadeau, J H, Tanzi, R E, Watkins, P C, Jagadesh, J, Taylor, B A, Haines, J L, Sacchi, N, Gusella, J F
Publicado em 1988

Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.

Por Whaley, W L, Michiels, F, MacDonald, M E, Romano, D, Zimmer, M, Smith, B, Leavitt, J, Bucan, M, Haines, J L, Gilliam, T C
Publicado em 1988

Localization of juvenile, but not late-infantile, neuronal ceroid lipofuscinosis on chromosome 16.

Por Yan, W, Boustany, R M, Konradi, C, Ozelius, L, Lerner, T, Trofatter, J A, Julier, C, Breakefield, X O, Gusella, J F, Haines, J L
Publicado em 1993

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity.

Por Haines, J L, Short, M P, Kwiatkowski, D J, Jewell, A, Andermann, E, Bejjani, B, Yang, C H, Gusella, J F, Amos, J A
Publicado em 1991