1994
Linkage Study of a Susceptibility Locus for Schizophrenia in the Pseudoautosomal Region
Barr C, Kennedy J, Pakstis A, Castiglione C, Kidd J, Wetterberg L, Kidd K. Linkage Study of a Susceptibility Locus for Schizophrenia in the Pseudoautosomal Region. Schizophrenia Bulletin 1994, 20: 277-286. PMID: 8085132, DOI: 10.1093/schbul/20.2.277.Peer-Reviewed Original Research
1991
Status of the search for a major genetic locus for affective disorder in the Old Order Amish
Pakstis A, Kidd J, Castiglione C, Kidd K. Status of the search for a major genetic locus for affective disorder in the Old Order Amish. Human Genetics 1991, 87: 475-483. PMID: 1879834, DOI: 10.1007/bf00197172.Peer-Reviewed Original Research
1990
Segregation and Linkage Analyses of Tourette's Syndrome and Related Disorders
PAULS D, PAKSTIS A, KURLAN R, KIDD K, LECKMAN J, COHEN D, KIDD J, COMO P, SPARKES R. Segregation and Linkage Analyses of Tourette's Syndrome and Related Disorders. Journal Of The American Academy Of Child & Adolescent Psychiatry 1990, 29: 195-203. PMID: 2324061, DOI: 10.1097/00004583-199003000-00007.Peer-Reviewed Original Research
1989
Closing in on the MEN2A locus.
Simpson N, Kidd K. Closing in on the MEN2A locus. Henry Ford Hospital Medical Journal 1989, 37: 100-5. PMID: 2576936.Peer-Reviewed Original Research
1981
Dermo‐distortive urticaria: An autosomal dominant dermatologic disorder
Epstein P, Kidd K, Opitz J. Dermo‐distortive urticaria: An autosomal dominant dermatologic disorder. American Journal Of Medical Genetics 1981, 9: 307-315. PMID: 7294069, DOI: 10.1002/ajmg.1320090407.Peer-Reviewed Original ResearchMeSH KeywordsChromosome AberrationsChromosome DisordersFemaleHumansMalePedigreePhenotypePhysical Education and TrainingUrticariaGenetic linkage analysis of dermo‐distortive urticaria
Epstein P, Kidd K, Sparkes R, Opitz J. Genetic linkage analysis of dermo‐distortive urticaria. American Journal Of Medical Genetics 1981, 9: 317-321. PMID: 6945804, DOI: 10.1002/ajmg.1320090408.Peer-Reviewed Original Research
1976
Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21
FINEMAN R, KIDD K, JOHNSON A, BREG W. Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21. Nature 1976, 260: 320-321. PMID: 1082990, DOI: 10.1038/260320a0.Peer-Reviewed Original Research