Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

R.S. Kandt, Jonathan L. Haines, M. Smith, +14

Nature Genetics

Mendelian DisorderGenetic DisorderGeneticsRenal PathologyImportant Gene Locus +8

Autism and the serotonin transporter: the long and short of it

Bernie Devlin, Edwin H. Cook, Hilary Coon, +9

Molecular Psychiatry

PsychopathologyPsychiatryBehavioral NeuroscienceSyndromic AutismAutism +9

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

Deborah Grady, H-C Chi, Y.-C. Ding, +7

Molecular Psychiatry

AdhdNeuropsychologyPsychiatryGenetic DisorderAttention-deficit Hyperactivity Disorder +9

Molecular analysis of the human class I alcohol dehydrogenase gene family and nucleotide sequence of the gene encoding the beta subunit.

Gregg Duester, M. Smith, Virginia Bilanchone, +1

Journal of Biological Chemistry

Evidence for multiple loci from a genome scan of autism kindreds

Gerard D. Schellenberg, Géraldine Dawson, Yun Ju Sung, +15

Molecular Psychiatry

Genome-wide Association StudySyndromic AutismGeneticsPsychiatric GeneticsMultiple Loci +7

Assignment of human alpha 1-antitrypsin to chromosome 14 by somatic cell hybrid analysis.

G.J. Darlington, Kenneth H. Astrin, S P Muirhead, +2

Proceedings of the National Academy of Sciences

Knockout MouseChromatinXenotransplantationHuman Parental CellsProtein Expression +13

Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qter.

Ai-li Wang, F X Arredondo-Vega, Philip F. Giampietro, +3

Proceedings of the National Academy of Sciences

Human Porphobilinogen DeaminaseGeneticsHuman Chromosome ComplementMolecular BiologyGene Characterization +17

Mild “Unstable Haemoglobin Haemolytic Anaemia” caused by Haemoglobin Shepherds Bush (B74 (E18) Gly→Asp)

Jason M. White, M. C. Brain, P.A. Lorkin, +2

Nature

ImmunohematologyLaboratory HematologyHeme DegradationHematologyVeterinary Science +4

Human placental and intestinal alkaline phosphatase genes map to 2q34-q37.

C.A. Griffin, M. Smith, Paula S. Henthorn, +4

PubMed

Phenotypic variation of tuberous sclerosis in a single extended kindred.

Susan L. Smalley, F J Burger, M. Smith

Journal of Medical Genetics

Family MembersGeneticsGenetic EpidemiologyPathologyMolecular Genetics +15