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Genomics|January 1, 1993
Twelve new polymorphic microsatellites on human chromosome 22J C Porter, K T Ram, J M PuckPediatric Research|January 1, 1993
Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disordersJ M PuckJournal of Clinical Immunology|March 1, 1994
Molecular and genetic basis of X-linked immunodeficiency disordersJ M PuckHuman Molecular Genetics|August 1, 1993
The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1J M Puck, S M Deschênes, J C Porter, et al.Current Opinion in Pediatrics|December 11, 1999
Autoimmune lymphoproliferative syndrome, a disorder of apoptosisC E Jackson, J M PuckAmerican Journal of Medical Genetics|June 28, 2001
Family pictures: growing up with a brother with X-linked severe combined immunodeficiencyJ H Fanos, J M PuckSeminars in Immunology|February 1, 1997
ALPS: an autoimmune human lymphoproliferative syndrome associated with abnormal lymphocyte apoptosisJ M Puck, M C SnellerThe Journal of Pediatrics|May 1, 1988
Carrier detection in typical and atypical X-linked agammaglobulinemiaM E Conley, J M PuckPageof 21