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H D Bakker

Showing results (1-10 of 85) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|April 17, 1982
[Terminal care in children]H D Bakker
Nederlands Tijdschrift Voor Geneeskunde|May 8, 1993
[Remember hereditary metabolic diseases in children in which no satisfactory diagnosis can be established]H D Bakker
Nederlands Tijdschrift Voor Geneeskunde|December 21, 1985
["Sugr makes me sick"]H D Bakker
Skeletal Radiology|January 1, 1984
Mucolipidosis I. Roentgenographic follow-upC R Staalman, H D Bakker
American Journal of Medical Genetics|June 13, 1997
Macrocephaly, facial abnormalities, disproportionate tall stature, and mental retardation--a sib observationH D Bakker, R C Hennekam
Nederlands Tijdschrift Voor Geneeskunde|October 11, 1980
[Current possibilities in the diagnosis and treatment of congenital metabolic diseases]H D Bakker, A H van Gennip
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 1, 1977
Some kinetic properites of liver ornithine carbamoyl transferase (OCT) in a patient with OCT deficiencyC van der Heiden, J Desplanque, H D Bakker
Tijdschrift Voor Kindergeneeskunde|April 1, 1985
[Type I tricho-rhino-phalangeal syndrome]S van Deursen, C R Staalman, H D Bakker
Tijdschrift Voor Kindergeneeskunde|February 1, 1992
[Severe complications following an adeno-tonsillectomy in a patient with Hunter's syndrome (MPS II)]R J Oostra, B I Beentjes, H D Bakker
Nederlands Tijdschrift Voor Geneeskunde|February 3, 2004
[From gene to disease; galactosemia and galactose-1-phosphate uridyltransferase deficiency]A M Bosch, H R Waterham, H D Bakker
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Nederlands Tijdschrift Voor Geneeskunde|April 17, 1982
[Terminal care in children]H D Bakker
Nederlands Tijdschrift Voor Geneeskunde|May 8, 1993
[Remember hereditary metabolic diseases in children in which no satisfactory diagnosis can be established]H D Bakker
Nederlands Tijdschrift Voor Geneeskunde|December 21, 1985
["Sugr makes me sick"]H D Bakker
Skeletal Radiology|January 1, 1984
Mucolipidosis I. Roentgenographic follow-upC R Staalman, H D Bakker
American Journal of Medical Genetics|June 13, 1997
Macrocephaly, facial abnormalities, disproportionate tall stature, and mental retardation--a sib observationH D Bakker, R C Hennekam
Nederlands Tijdschrift Voor Geneeskunde|October 11, 1980
[Current possibilities in the diagnosis and treatment of congenital metabolic diseases]H D Bakker, A H van Gennip
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 1, 1977
Some kinetic properites of liver ornithine carbamoyl transferase (OCT) in a patient with OCT deficiencyC van der Heiden, J Desplanque, H D Bakker
Tijdschrift Voor Kindergeneeskunde|April 1, 1985
[Type I tricho-rhino-phalangeal syndrome]S van Deursen, C R Staalman, H D Bakker
Tijdschrift Voor Kindergeneeskunde|February 1, 1992
[Severe complications following an adeno-tonsillectomy in a patient with Hunter's syndrome (MPS II)]R J Oostra, B I Beentjes, H D Bakker
Nederlands Tijdschrift Voor Geneeskunde|February 3, 2004
[From gene to disease; galactosemia and galactose-1-phosphate uridyltransferase deficiency]A M Bosch, H R Waterham, H D Bakker
Pageof 9