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Magnetic Resonance in Medicine|April 1, 1986
A new method for flow velocity measurement: frequency encoded NMRA Caprihan, J G Davis, S A Altobelli, et al.Clinical Genetics|March 1, 1979
Prenatal diagnosis of trisomy 20 mosaicismN B Kardon, E Lieber, J G Davis, et al.Environmental Science & Technology|February 18, 2010
Identification of antibiotic-resistance-gene molecular signatures suitable as tracers of pristine river, urban, and agricultural sourcesH Storteboom, M Arabi, J G Davis, et al.Human Genetics|February 1, 1980
Incidence of chromosomal rearrangements in couples with reproductive lossN B Kardon, J G Davis, A L Berger, et al.Haematologia|January 1, 1989
A second case of neonatal alloimmune thrombocytopenia associated with anti-PlA2 (Zwb) antibodiesK Maslanka, G F Lucas, A Gronkowska, et al.American Journal of Medical Genetics|January 10, 1997
Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry StudyP F Giampietro, P C Verlander, J G Davis, et al.British Journal of Haematology|August 1, 1987
Pre-transfusion non-invasive quality assessment of stored platelet concentratesE L Bellhouse, M J Inskip, J G Davis, et al.Science (New York, N.Y.)|February 17, 1995
Molecular cloning and characterization of an inner ear-specific structural proteinJ G Davis, J C Oberholtzer, F R Burns, et al.Cytogenetics and Cell Genetics|January 1, 1976
A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-J G Davis, E C Jenkins, H P Klinger, et al.American Journal of Medical Genetics. Supplement|January 1, 1987
Berry aneurysms, cirrhosis, pulmonary emphysema, and bilateral symmetrical cerebral calcifications: a new syndromeE Kahn, J Markowitz, L Duffy, et al.Pageof 7