L. Larson

Further evidence by gene dosage for the regional assignment of erythrocyte acid phosphatase (ACPI) and malate dehydrogenase (MDHI) loci on chromosome 2p

L. Larson, A. Bruce, J. Saumur, 1982, Clinical genetics.

Chromosome abnormality in Kallmann syndrome.

L. Larson, L. Best, W. Wasdahl, 1990, American journal of medical genetics.

Partial trisomy 7p associated with familial 7p;22q translocation.

L. Larson, S. Jalal, W. Wasdahl, 1977, Journal of medical genetics.

Complete trisomy 17p a relatively new syndrome.

L. Larson, S. Jalal, M. Kukolich, 1988, Annales de genetique.

Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

L. Larson, J. Saumur, S. Jalal, 1978, Journal of medical genetics.

Familial reciprocal translocation, t(2;10)(p24;q26), resulting in duplication 2p and deletion 10q

L. Larson, M. Coleman, C. Dolan, 1982, Clinical genetics.

Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation.

L. Burd, J. Kerbeshian, L. Larson, 2000, American journal of medical genetics.