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R D Blackston

Showing results (1-10 of 15) with videos related to

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Journal of Medical Genetics|June 1, 1972
A case of 48,XXXX female with normal intelligenceR D Blackston, A T Chen
The Journal of Pediatrics|May 1, 1977
Parental mosaicism as a cause of Down syndrome. A report of 46,XX/46,XX,--21,+t(21q21q1 mother and 46,XY,+21,+t(21q21q) childJ H Priest, K E Brantley, R D Blackston
The Journal of Clinical Endocrinology and Metabolism|March 1, 1979
Predicting the response of growth hormone-deficient children to long term treatment with human growth hormoneD Rudman, M H Kutner, M A Goldsmith, et al.
Human Genetics|December 1, 1988
Molecular evidence for true isochromosome 21qJ H Priest, R D Blackston, L A Pearse, et al.
Journal of Medical Genetics|December 1, 1975
Differences in human X isochromosomesJ H Priest, R D Blackston, K S Au, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1981
Epinephrine deficiency in hypocorticotropic hypopituitary childrenD Rudman, S D Moffitt, P M Fernhoff, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1979
Normal variant short stature: subclassification based on responses to exogenous human growth hormoneD Rudman, M H Kutner, R D Blackston, et al.
American Journal of Medical Genetics|February 2, 1996
Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)]S B Freeman, K Muralidharan, D Pettay, et al.
The Journal of Clinical Investigation|December 1, 1979
Serum and urine polyamines in normal and in short childrenD Rudman, M H Kutner, R K Chawla, et al.
The New England Journal of Medicine|July 16, 1981
Children with normal-variant short stature: treatment with human growth hormone for six monthsD Rudman, M H Kutner, R D Blackston, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|June 1, 1972
A case of 48,XXXX female with normal intelligenceR D Blackston, A T Chen
The Journal of Pediatrics|May 1, 1977
Parental mosaicism as a cause of Down syndrome. A report of 46,XX/46,XX,--21,+t(21q21q1 mother and 46,XY,+21,+t(21q21q) childJ H Priest, K E Brantley, R D Blackston
The Journal of Clinical Endocrinology and Metabolism|March 1, 1979
Predicting the response of growth hormone-deficient children to long term treatment with human growth hormoneD Rudman, M H Kutner, M A Goldsmith, et al.
Human Genetics|December 1, 1988
Molecular evidence for true isochromosome 21qJ H Priest, R D Blackston, L A Pearse, et al.
Journal of Medical Genetics|December 1, 1975
Differences in human X isochromosomesJ H Priest, R D Blackston, K S Au, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1981
Epinephrine deficiency in hypocorticotropic hypopituitary childrenD Rudman, S D Moffitt, P M Fernhoff, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1979
Normal variant short stature: subclassification based on responses to exogenous human growth hormoneD Rudman, M H Kutner, R D Blackston, et al.
American Journal of Medical Genetics|February 2, 1996
Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)]S B Freeman, K Muralidharan, D Pettay, et al.
The Journal of Clinical Investigation|December 1, 1979
Serum and urine polyamines in normal and in short childrenD Rudman, M H Kutner, R K Chawla, et al.
The New England Journal of Medicine|July 16, 1981
Children with normal-variant short stature: treatment with human growth hormone for six monthsD Rudman, M H Kutner, R D Blackston, et al.
Pageof 2