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G N Donnell

Showing results (11-20 of 73) with videos related to

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Birth Defects Original Article Series|January 1, 1976
The 9p--syndromeO S Alfi, G N Donnell, A Derencsenyi
Pediatrics|September 1, 1971
Quinacrine fluoromicroscopy in the identification of human mitotic chromosomesO S Alfi, G N Donnell, A Derencsenyi
JAMA|January 9, 1987
Transferase-deficiency galactosemia and the Duarte variantW G Ng, J S Lee, G N Donnell
Birth Defects Original Article Series|January 1, 1976
The dietary prophylaxis of cataracts in patients with galactosemiaW A Wilson, G N Donnell, W R Bergren
Human Genetics|January 1, 1985
Identification of a case of Y:18 translocation using a Y-specific repetitive DNA probeY F Lau, K L Ying, G N Donnell
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1975
Mannitol excretion in galactosemia patientsW G Ng, G N Donnell, W R Bergren
Journal of Inherited Metabolic Disease|January 1, 1978
Prenatal diagnosis and a case report of isovaleric acidaemiaM E Blaskovics, W G Ng, G N Donnell
Journal of Inherited Metabolic Disease|January 1, 1990
Long-term prognosis in galactosaemia: results of a survey of 350 casesD D Waggoner, N R Buist, G N Donnell
Fertility and Sterility|June 1, 1987
Ovarian androgen secretion in patients with galactosemia and premature ovarian failureF R Kaufman, G N Donnell, R A Lobo
Clinical Pediatrics|January 1, 1980
Developmental aspects of galactosemia from infancy to childhoodK Fishler, R Koch, G N Donnell, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
Birth Defects Original Article Series|January 1, 1976
The 9p--syndromeO S Alfi, G N Donnell, A Derencsenyi
Pediatrics|September 1, 1971
Quinacrine fluoromicroscopy in the identification of human mitotic chromosomesO S Alfi, G N Donnell, A Derencsenyi
JAMA|January 9, 1987
Transferase-deficiency galactosemia and the Duarte variantW G Ng, J S Lee, G N Donnell
Birth Defects Original Article Series|January 1, 1976
The dietary prophylaxis of cataracts in patients with galactosemiaW A Wilson, G N Donnell, W R Bergren
Human Genetics|January 1, 1985
Identification of a case of Y:18 translocation using a Y-specific repetitive DNA probeY F Lau, K L Ying, G N Donnell
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1975
Mannitol excretion in galactosemia patientsW G Ng, G N Donnell, W R Bergren
Journal of Inherited Metabolic Disease|January 1, 1978
Prenatal diagnosis and a case report of isovaleric acidaemiaM E Blaskovics, W G Ng, G N Donnell
Journal of Inherited Metabolic Disease|January 1, 1990
Long-term prognosis in galactosaemia: results of a survey of 350 casesD D Waggoner, N R Buist, G N Donnell
Fertility and Sterility|June 1, 1987
Ovarian androgen secretion in patients with galactosemia and premature ovarian failureF R Kaufman, G N Donnell, R A Lobo
Clinical Pediatrics|January 1, 1980
Developmental aspects of galactosemia from infancy to childhoodK Fishler, R Koch, G N Donnell, et al.
Pageof 8