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P M Fernhoff

Showing results (31-40 of 45) with videos related to

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American Journal of Medical Genetics|July 11, 1997
Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992H E Roberts, C A Moore, P M Fernhoff, et al.
Journal of Medical Genetics|October 1, 1976
Association of D/D translocations with fetal wastage and aneuploidy. A report of four familiesP M Fernhoff, D N Singh, J Hanson, et al.
American Journal of Medical Genetics|March 29, 1996
Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infantH E Roberts, D F Saxe, K Muralidharan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1981
The relation between growth velocity and serum somatomedin C concentrationD Rudman, S D Moffitt, P M Fernhoff, et al.
American Journal of Obstetrics and Gynecology|March 1, 1988
Prenatal diagnosis of 21-hydroxylase deficiency by the complementary deoxyribonucleic acid probe for cytochrome P-450C-21OHR H Reindollar, J B Lewis, P C White, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiencyF Scaglia, Y Wang, R H Singh, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|September 1, 1981
Zinc and copper status of treated children with phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Zinc status and growth of children undergoing treatment for phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Pediatric Dermatology|March 13, 1998
Lymphedema as a postulated cause of cutis verticis gyrata in Turner syndromeM Larralde, S S Gardner, M V Torrado, et al.
Pediatric Research|October 1, 1985
Thiamine response in maple syrup urine diseaseP M Fernhoff, D Lubitz, D J Danner, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|July 11, 1997
Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992H E Roberts, C A Moore, P M Fernhoff, et al.
Journal of Medical Genetics|October 1, 1976
Association of D/D translocations with fetal wastage and aneuploidy. A report of four familiesP M Fernhoff, D N Singh, J Hanson, et al.
American Journal of Medical Genetics|March 29, 1996
Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infantH E Roberts, D F Saxe, K Muralidharan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1981
The relation between growth velocity and serum somatomedin C concentrationD Rudman, S D Moffitt, P M Fernhoff, et al.
American Journal of Obstetrics and Gynecology|March 1, 1988
Prenatal diagnosis of 21-hydroxylase deficiency by the complementary deoxyribonucleic acid probe for cytochrome P-450C-21OHR H Reindollar, J B Lewis, P C White, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 23, 2001
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiencyF Scaglia, Y Wang, R H Singh, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|September 1, 1981
Zinc and copper status of treated children with phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Zinc status and growth of children undergoing treatment for phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Pediatric Dermatology|March 13, 1998
Lymphedema as a postulated cause of cutis verticis gyrata in Turner syndromeM Larralde, S S Gardner, M V Torrado, et al.
Pediatric Research|October 1, 1985
Thiamine response in maple syrup urine diseaseP M Fernhoff, D Lubitz, D J Danner, et al.
Pageof 5