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M A Preece

Showing results (241-250 of 250) with videos related to

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Journal of Inherited Metabolic Disease|June 12, 2009
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UKT Hutchin, M A Preece, C Hendriksz, et al.
Archives of Disease in Childhood|December 1, 1976
Clinical and subclinical vitamin D deficiency in Bradford childrenJ A Ford, W V McIntosh, R Butterfield, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1993
Clinical features and endocrine status in patients with growth hormone insensitivity (Laron syndrome)M O Savage, W F Blum, M B Ranke, et al.
Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Phenotype: genotype relationships in growth hormone insensitivity syndromeK A Woods, F Dastot, M A Preece, et al.
Scientific Reports|November 19, 2020
Radiographic characterisation of spinal curvature development in farmed New Zealand Chinook salmon Oncorhynchus tshawytscha throughout seawater productionB A Lovett, E C Firth, I D Tuck, et al.
Archives of Disease in Childhood|January 25, 2002
Growth reference charts for use in the United KingdomC M Wright, I W Booth, J M H Buckler, et al.
Clinical Endocrinology|July 1, 1979
Experience with human growth hormone in Great Britain: the report of the MRC Working PartyR D Milner, T Russell-Fraser, C G Brook, et al.
American Journal of Human Genetics|February 15, 2001
Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?S Mergenthaler, M P Hitchins, N Blagitko-Dorfs, et al.
Hormone Research|September 11, 2001
Clinical and endocrine characteristics in atypical and classical growth hormone insensitivity syndromeC P Burren, K A Woods, S J Rose, et al.
Pageof 25

Showing results (241-250 of 250) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 250 results.
Journal of Inherited Metabolic Disease|June 12, 2009
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UKT Hutchin, M A Preece, C Hendriksz, et al.
Archives of Disease in Childhood|December 1, 1976
Clinical and subclinical vitamin D deficiency in Bradford childrenJ A Ford, W V McIntosh, R Butterfield, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1993
Clinical features and endocrine status in patients with growth hormone insensitivity (Laron syndrome)M O Savage, W F Blum, M B Ranke, et al.
Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Phenotype: genotype relationships in growth hormone insensitivity syndromeK A Woods, F Dastot, M A Preece, et al.
Scientific Reports|November 19, 2020
Radiographic characterisation of spinal curvature development in farmed New Zealand Chinook salmon Oncorhynchus tshawytscha throughout seawater productionB A Lovett, E C Firth, I D Tuck, et al.
Archives of Disease in Childhood|January 25, 2002
Growth reference charts for use in the United KingdomC M Wright, I W Booth, J M H Buckler, et al.
Clinical Endocrinology|July 1, 1979
Experience with human growth hormone in Great Britain: the report of the MRC Working PartyR D Milner, T Russell-Fraser, C G Brook, et al.
American Journal of Human Genetics|February 15, 2001
Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?S Mergenthaler, M P Hitchins, N Blagitko-Dorfs, et al.
Hormone Research|September 11, 2001
Clinical and endocrine characteristics in atypical and classical growth hormone insensitivity syndromeC P Burren, K A Woods, S J Rose, et al.
Pageof 25