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C M Hall

Showing results (151-160 of 188) with videos related to

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Hormone Research|January 4, 2005
Female preponderance in congenital adrenal hyperplasia due to CYP21 deficiency in England: implications for neonatal screeningA Nordenström, S Ahmed, J Jones, et al.
Clinical Endocrinology|June 1, 1997
Serum leptin through childhood and adolescenceP E Clayton, M S Gill, C M Hall, et al.
Pediatric Neurosurgery|July 1, 1996
Congenital cervical spinal fusion: a study in Apert syndromeD N Thompson, S F Slaney, C M Hall, et al.
The Journal of Craniofacial Surgery|July 1, 1996
Cervical spine in Pfeiffer's syndromeP J Anderson, C M Hall, R D Evans, et al.
Hormone Research|March 16, 2007
Efficacy of a monthly compared to 3-monthly depot GnRH analogue (goserelin) in the treatment of children with central precocious pubertyH Isaac, L Patel, S Meyer, et al.
Journal of Medical Genetics|December 20, 2003
Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypesJ C Oosterwijk, S Mansour, G van Noort, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delayP T Clayton, S Eckhardt, J Wilson, et al.
Journal of Medical Genetics|March 19, 2002
Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndromeJ A Goodship, J O'Sullivan, P F Chinnery, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 1, 1997
The cervical spine in Saethre-Chotzen syndromeP J Anderson, C M Hall, R D Evans, et al.
Clinical Dysmorphology|May 8, 1998
Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndromeE M Rosser, H Kaariainen, J A Hurst, et al.
Pageof 19

Showing results (151-160 of 188) with videos related to

Sort By:
Pageof 19
Hormone Research|January 4, 2005
Female preponderance in congenital adrenal hyperplasia due to CYP21 deficiency in England: implications for neonatal screeningA Nordenström, S Ahmed, J Jones, et al.
Clinical Endocrinology|June 1, 1997
Serum leptin through childhood and adolescenceP E Clayton, M S Gill, C M Hall, et al.
Pediatric Neurosurgery|July 1, 1996
Congenital cervical spinal fusion: a study in Apert syndromeD N Thompson, S F Slaney, C M Hall, et al.
The Journal of Craniofacial Surgery|July 1, 1996
Cervical spine in Pfeiffer's syndromeP J Anderson, C M Hall, R D Evans, et al.
Hormone Research|March 16, 2007
Efficacy of a monthly compared to 3-monthly depot GnRH analogue (goserelin) in the treatment of children with central precocious pubertyH Isaac, L Patel, S Meyer, et al.
Journal of Medical Genetics|December 20, 2003
Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypesJ C Oosterwijk, S Mansour, G van Noort, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delayP T Clayton, S Eckhardt, J Wilson, et al.
Journal of Medical Genetics|March 19, 2002
Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndromeJ A Goodship, J O'Sullivan, P F Chinnery, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 1, 1997
The cervical spine in Saethre-Chotzen syndromeP J Anderson, C M Hall, R D Evans, et al.
Clinical Dysmorphology|May 8, 1998
Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndromeE M Rosser, H Kaariainen, J A Hurst, et al.
Pageof 19