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Genetic Heterogeneity in Tuberous Sclerosis.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 274, doi. 10.1111/j.1749-6632.1991.tb37769.x
By:
- SMITH, MOYRA;
- YOSHIYAMA, K.;
- WAGNER, C.;
- FLODMAN, P.;
- SMITH, B.
Publication type:
Article
Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataseta.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 256, doi. 10.1111/j.1749-6632.1991.tb37767.x
By:
- HAINES, J. L.;
- AMOS, J.;
- ATTWOOD, J.;
- BECH-HANSEN, N. T.;
- BURLEY, M.;
- CONNEALLY, P. M.;
- CONNOR, J. M.;
- FAHSOLD, R.;
- FLODMAN, P.;
- FRYER, A.;
- HALLEY, D. J. J.;
- JEWELL, A.;
- JANSSEN, L. A. J.;
- KANDT, R.;
- NORTHRUP, H.;
- OSBORNE, J.;
- PERICAK-VANCE, M.;
- POVEY, S.;
- SAMPSON, J.;
- SHORT, M. P.
Publication type:
Article
An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methodsa.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 298, doi. 10.1111/j.1749-6632.1991.tb37771.x
By:
- POVEY, S.;
- ATTWOOD, J.;
- JANSSEN, L. A. J.;
- BURLEY, M.;
- SMITH, M.;
- FLODMAN, P.;
- MORTON, N. E.;
- EDWARDS, J. H.;
- SAMPSON, J. R.;
- YATES, J. R. W.;
- HAINES, J. L.;
- AMOS, J.;
- SHORT, M. P.;
- SANDKUYL, L. A.;
- HALLEY, D. J. J.;
- FRYER, A. E.;
- BECH-HANSEN, T.;
- MUELLER, R.;
- AL-GHAZALI, L.;
- SUPER, M.
Publication type:
Article
A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22-23a.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 306, doi. 10.1111/j.1749-6632.1991.tb37772.x
By:
- JANSSEN, L. A. J.;
- POVEY, S.;
- ATTWOOD, J.;
- SANDKUYL, L. A.;
- LINDHOUT, D.;
- FLODMAN, P.;
- SMITH, M.;
- SAMPSON, J. R.;
- HAINES, J. L.;
- MERKENS, E. C.;
- FLEURY, P.;
- SHORT, P.;
- AMOS, J.;
- HALLEY, D. J. J.
Publication type:
Article
Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population.
Published in:
2002
By:
- Neiswanger, K.;
- Cooper, M.E.;
- Weinberg, S M;
- Flodman, P;
- Keglovits, A Bundens;
- Liu, Y;
- Hu, D N;
- Melnick, M;
- Spence, M A;
- Marazita, M L
Publication type:
journal article
Language and other regression: assessment and timing.
Published in:
2003
By:
- Goldberg WA;
- Osann K;
- Filipek PA;
- Laulhere T;
- Jarvis K;
- Modahl C;
- Flodman P;
- Spence MA
Publication type:
Journal Article
Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.
Published in:
Cytogenetics & Cell Genetics, 2001, v. 94, n. 1/2, p. 15, doi. 10.1159/000048775
By:
- Smith, M.;
- Escamilla, J. R.;
- Filipek, P.;
- Bocian, M. E.;
- Modahi, C.;
- Flodman, P.;
- Spence, M. A.
Publication type:
Article
Bayesian risk assessment in genetic testing for autosomal dominant disorders with age-dependent penetrance.
Published in:
2007
By:
- Ogino S;
- Wilson RB;
- Gold B;
- Flodman P
Publication type:
Journal Article
Evidence for multiple loci from a genome scan of autism kindreds.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 11, p. 1049, doi. 10.1038/sj.mp.4001874
By:
- Schellenberg, G. D.;
- Dawson, G.;
- Sung, Y. J.;
- Estes, A.;
- Munson, J.;
- Rosenthal, E.;
- Rothstein, J.;
- Flodman, P.;
- Smith, M.;
- Coon, H.;
- Leong, L.;
- Yu, C.-E.;
- Stodgell, C.;
- Rodier, P. M.;
- Spence, M. A.;
- Minshew, N.;
- McMahon, W. M.;
- Wijsman, E. M.
Publication type:
Article
Evidence for genetic linkage of autism to chromosomes 7 and 4.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 11, p. 979, doi. 10.1038/sj.mp.4001918
By:
- Schellenberg, G. D.;
- Dawson, G.;
- Sung, Y. J.;
- Estes, A.;
- Munson, J.;
- Rosenthal, E.;
- Rothstein, J.;
- Flodman, P.;
- Smith, M.;
- Coon, H.;
- Leong, L.;
- Yu, C.-E.;
- Stodgell, C.;
- Rodier, P. M.;
- Spence, M. A.;
- Minshew, N.;
- McMahon, W. M.;
- Wijsman, E. M.
Publication type:
Article
High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 5, p. 536, doi. 10.1038/sj.mp.4001350
By:
- Grady, D L;
- Chi, H-C;
- Ding, Y-C;
- Smith, M;
- Wang, E;
- Schuck, S;
- Flodman, P;
- Spence, M A;
- Swanson, J M;
- Moyzis, R K
Publication type:
Article

Found: 11

Genetic Heterogeneity in Tuberous Sclerosis.

Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset<sup>a</sup>.

An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methods<sup>a</sup>.

A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22-23<sup>a</sup>.

Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population.

Language and other regression: assessment and timing.

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR.

Bayesian risk assessment in genetic testing for autosomal dominant disorders with age-dependent penetrance.

Evidence for multiple loci from a genome scan of autism kindreds.

Evidence for genetic linkage of autism to chromosomes 7 and 4.

High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.