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L J Sheffield

Showing results (31-40 of 61) with videos related to

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Prenatal Diagnosis|September 22, 1998
Fetal outcome and maternal morbidity after early amniocentesisV R Collins, C Webley, L J Sheffield, et al.
The Journal of Pediatrics|March 1, 1976
Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemiaL J Sheffield, D M Danks, J W Hammond, et al.
Human Genetics|March 1, 1988
Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration familiesJ C Mulley, E A Haan, L J Sheffield, et al.
The Medical Journal of Australia|August 7, 1989
Analysis of DNA probes for the prenatal diagnosis of cystic fibrosisP J Dry, S Wake, C F Robertson, et al.
Genetic Epidemiology|December 22, 1999
A more powerful method to evaluate p-values in GENEHUNTERH Zhao, L J Sheffield, A J Pakstis, et al.
Genetic Epidemiology|December 22, 1999
Analyses of the COGA data set in one ethnic group with examinations of alternative definitions of alcoholismL J Sheffield, M P Knauert, A J Pakstis, et al.
Prenatal Diagnosis|May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined populationJ L Halliday, L F Watson, J Lumley, et al.
Australian Dental Journal|December 1, 1992
Binder's syndrome due to prenatal vitamin K deficiency: a theory of pathogenesisA M Howe, W S Webster, A H Lipson, et al.
Molecular Genetics and Metabolism|December 23, 1999
Late diagnosis of maternal PKU in a family segregating an arylsulfatase [corrected] E mutation causing symmetrical chondrodysplasia punctataH H Dahl, A H Osborn, W M Hutchison, et al.
American Journal of Obstetrics and Gynecology|February 1, 1983
A clinical approach to the use of predictive values in the prenatal diagnosis of neural tube defectsL J Sheffield, D L Sackett, C H Goldsmith, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|September 22, 1998
Fetal outcome and maternal morbidity after early amniocentesisV R Collins, C Webley, L J Sheffield, et al.
The Journal of Pediatrics|March 1, 1976
Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemiaL J Sheffield, D M Danks, J W Hammond, et al.
Human Genetics|March 1, 1988
Recombination frequencies between Duchenne muscular dystrophy and intragenic markers in multigeneration familiesJ C Mulley, E A Haan, L J Sheffield, et al.
The Medical Journal of Australia|August 7, 1989
Analysis of DNA probes for the prenatal diagnosis of cystic fibrosisP J Dry, S Wake, C F Robertson, et al.
Genetic Epidemiology|December 22, 1999
A more powerful method to evaluate p-values in GENEHUNTERH Zhao, L J Sheffield, A J Pakstis, et al.
Genetic Epidemiology|December 22, 1999
Analyses of the COGA data set in one ethnic group with examinations of alternative definitions of alcoholismL J Sheffield, M P Knauert, A J Pakstis, et al.
Prenatal Diagnosis|May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined populationJ L Halliday, L F Watson, J Lumley, et al.
Australian Dental Journal|December 1, 1992
Binder's syndrome due to prenatal vitamin K deficiency: a theory of pathogenesisA M Howe, W S Webster, A H Lipson, et al.
Molecular Genetics and Metabolism|December 23, 1999
Late diagnosis of maternal PKU in a family segregating an arylsulfatase [corrected] E mutation causing symmetrical chondrodysplasia punctataH H Dahl, A H Osborn, W M Hutchison, et al.
American Journal of Obstetrics and Gynecology|February 1, 1983
A clinical approach to the use of predictive values in the prenatal diagnosis of neural tube defectsL J Sheffield, D L Sackett, C H Goldsmith, et al.
Pageof 7