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S J Moedjono

Showing results (1-10 of 9) with videos related to

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Human Genetics|September 1, 1979
Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)matS J Moedjono, R S Sparkes
Annales De Genetique|January 1, 1980
Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?S J Moedjono, R S Sparkes
American Journal of Mental Deficiency|May 1, 1983
Language abnormalities and minimal physical anomalies in a boy with partial trisomy of chromosome 15S J Moedjono, R Needleman, S J Funderburk
The New England Journal of Medicine|May 18, 1978
Normal karyotypes in infants with neural-tube defectsM A Fishman, S J Moedjono, K Taysi
Journal of Medical Genetics|June 1, 1980
Tetrasomy 9p: confirmation by enzyme analysisS J Moedjono, B F Crandall, R S Sparkes
Journal of Medical Genetics|October 1, 1979
18p--syndrome resulting from translocation (13a;18q) in a mildly affected adult maleS J Moedjono, S J Funderburk, R S Sparkes
Human Genetics|October 19, 1978
Chromosome 7 short-arm interstitial deletion (p14)S J Moedjono, S J Funderburk, R S Sparkes
Journal of Inherited Metabolic Disease|January 1, 1982
Treatment of hyperargininaemia due to arginase deficiency with a chemically defined dietS D Cederbaum, S J Moedjono, K N Shaw, et al.
Clinical Genetics|December 1, 1980
The campomelic syndrome in a singleton and monozygotic twinsS J Moedjono, B F Crandall, R S Sparkes, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Genetics|September 1, 1979
Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)matS J Moedjono, R S Sparkes
Annales De Genetique|January 1, 1980
Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?S J Moedjono, R S Sparkes
American Journal of Mental Deficiency|May 1, 1983
Language abnormalities and minimal physical anomalies in a boy with partial trisomy of chromosome 15S J Moedjono, R Needleman, S J Funderburk
The New England Journal of Medicine|May 18, 1978
Normal karyotypes in infants with neural-tube defectsM A Fishman, S J Moedjono, K Taysi
Journal of Medical Genetics|June 1, 1980
Tetrasomy 9p: confirmation by enzyme analysisS J Moedjono, B F Crandall, R S Sparkes
Journal of Medical Genetics|October 1, 1979
18p--syndrome resulting from translocation (13a;18q) in a mildly affected adult maleS J Moedjono, S J Funderburk, R S Sparkes
Human Genetics|October 19, 1978
Chromosome 7 short-arm interstitial deletion (p14)S J Moedjono, S J Funderburk, R S Sparkes
Journal of Inherited Metabolic Disease|January 1, 1982
Treatment of hyperargininaemia due to arginase deficiency with a chemically defined dietS D Cederbaum, S J Moedjono, K N Shaw, et al.
Clinical Genetics|December 1, 1980
The campomelic syndrome in a singleton and monozygotic twinsS J Moedjono, B F Crandall, R S Sparkes, et al.
Pageof 1