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American Journal of Medical Genetics|March 1, 1990
Chromosome abnormality in Kallmann syndromeL G Best, W A Wasdahl, L M Larson, et al.Journal of Medical Genetics|August 1, 1977
Partial trisomy 7p associated with familial 7p;22q translocationL M Larson, W A Wasdahl, S M JalalClinical Genetics|October 1, 1982
Further evidence by gene dosage for the regional assignment of erythrocyte acid phosphatase (ACP1) and malate dehydrogenase (MDH1) loci on chromosome 2pL M Larson, A W Bruce, J H Saumur, et al.Journal of Medical Genetics|February 1, 1978
Trisomy 18 syndrome with an unusual karyotype: possible double isochromosomeL M Larson, W A Wasdahl, J H Saumur, et al.The American Journal of Gastroenterology|February 1, 1978
Mucinous carcinoid and endometriosis in an inside-out appendixM A Rodriguez, W A WasdahlClinical Genetics|March 1, 1982
Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and delection 10qL M Larson, W A Wasdahl, J H Saumur, et al.Clinical Cardiology|January 1, 1992
Fibroelastic papilloma arising in a Chiari networkD A Wasdahl, W A Wasdahl, W D EdwardsAmerican Journal of Medical Genetics|August 1, 1991
Familial posterior helical ear pits and Wiedemann-Beckwith syndromeL G BestClinical Genetics|June 1, 1987
Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) matJ T Martsolf, T R Chase, S M Jalal, et al.American Journal of Medical Genetics|February 1, 1983
Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocationT R Chase, S M Jalal, J T Martsolf, et al.Pageof 3