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I K Brandt

Showing results (1-10 of 28) with videos related to

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The Journal of the Indiana State Medical Association|March 1, 1978
PKU and hypothyroidism: blood test for newborn infantsI K Brandt
The Journal of the Indiana State Medical Association|April 1, 1973
Phenylketonuria--a continuing problemI K Brandt
The Journal of the Indiana State Medical Association|August 1, 1976
Screening for genetic disordersI K Brandt
Pediatric Research|June 1, 1976
Hurler syndrome: alpha-L-iduronidase activity in leukocytes as a method for heterozygote detectionR S Wappner, I K Brandt
Clinical Genetics|May 1, 1977
Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasiaV Escobar, I K Brandt, D Bixler
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1979
Structural comparison of hexosaminidases in primatesJ E Lee, A Yoshida, I K Brandt
Pediatric Research|August 1, 1978
White cell ornithine transcarbamylase activity cannot detect the liver enzyme deficiencyP J Snodgrass, R S Wappner, I K Brandt
Neurology|February 1, 1982
Nonketotic hyperglycinemia: electroencephalographic and evoked potential abnormalitiesO N Markand, B P Garg, I K Brandt
AJR. American Journal of Roentgenology|January 1, 1977
Acrodysostosis coinciding with pseudohypoparathyroidism and pseudo-pseudohypoparathyroidismR C Ablow, Y E Hsia, I K Brandt
American Journal of Medical Genetics|January 1, 1981
Kaufman syndrome (hydrometrocolpos, polydactyly, and congenital heart disease) with pituitary dysplasia, choanal atresia, and vertebral anomaliesJ C Knowles, I K Brandt, M J Bull
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
The Journal of the Indiana State Medical Association|March 1, 1978
PKU and hypothyroidism: blood test for newborn infantsI K Brandt
The Journal of the Indiana State Medical Association|April 1, 1973
Phenylketonuria--a continuing problemI K Brandt
The Journal of the Indiana State Medical Association|August 1, 1976
Screening for genetic disordersI K Brandt
Pediatric Research|June 1, 1976
Hurler syndrome: alpha-L-iduronidase activity in leukocytes as a method for heterozygote detectionR S Wappner, I K Brandt
Clinical Genetics|May 1, 1977
Unusual association of Saethre-Chotzen syndrome and congenital adrenal hyperplasiaV Escobar, I K Brandt, D Bixler
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1979
Structural comparison of hexosaminidases in primatesJ E Lee, A Yoshida, I K Brandt
Pediatric Research|August 1, 1978
White cell ornithine transcarbamylase activity cannot detect the liver enzyme deficiencyP J Snodgrass, R S Wappner, I K Brandt
Neurology|February 1, 1982
Nonketotic hyperglycinemia: electroencephalographic and evoked potential abnormalitiesO N Markand, B P Garg, I K Brandt
AJR. American Journal of Roentgenology|January 1, 1977
Acrodysostosis coinciding with pseudohypoparathyroidism and pseudo-pseudohypoparathyroidismR C Ablow, Y E Hsia, I K Brandt
American Journal of Medical Genetics|January 1, 1981
Kaufman syndrome (hydrometrocolpos, polydactyly, and congenital heart disease) with pituitary dysplasia, choanal atresia, and vertebral anomaliesJ C Knowles, I K Brandt, M J Bull
Pageof 3