J H Levin|S G Kaler - JoVE Visualize

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Clinical Genetics|August 16, 2005

Copper-replacement treatment for symptomatic Menkes disease: ethical considerationsS R Sheela, M Latha, P Liu, et al.

Annals of Neurology|February 1, 1993

Plasma and cerebrospinal fluid neurochemical pattern in Menkes diseaseS G Kaler, D S Goldstein, C Holmes, et al.

Clinical Genetics|May 26, 2010

Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes diseaseV Desai, A Donsante, K J Swoboda, et al.

American Journal of Medical Genetics|April 1, 1983

Brief clinical report: two children with de novo del(9p)R S Young, P Bader, C G Palmer, et al.

Genetic Testing|August 23, 2000

Novel method for molecular detection of the two common hereditary hemochromatosis mutationsS G Kaler, J M Devaney, E L Pettit, et al.

British Medical Bulletin|April 1, 1993

Travel vaccines--a review of current thinkingJ H Levin, P D Clarke

American Journal of Medical Genetics|October 2, 1996

Distinctive Menkes disease variant with occipital horns: delineation of natural history and clinical phenotypeV K Proud, H G Mussell, S G Kaler, et al.

Pediatric Research|February 1, 1994

Metallothionein synthesis and degradation in Indian childhood cirrhosis fibroblastsS H Hahn, M L Brantly, C Oliver, et al.

Fertility and Sterility|October 1, 1991

Is the inappropriate gonadotropin secretion of patients with polycystic ovary syndrome similar to that of patients with adult-onset congenital adrenal hyperplasia?J H Levin, E Carmina, R A Lobo

Analytical Chemistry|February 24, 2001

Genotyping of two mutations in the HFE gene using single-base extension and high-performance liquid chromatographyJ M Devaney, E L Pettit, S G Kaler, et al.

Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:

Pageof 4

Clinical Genetics|August 16, 2005

Copper-replacement treatment for symptomatic Menkes disease: ethical considerationsS R Sheela, M Latha, P Liu, et al.

Annals of Neurology|February 1, 1993

Plasma and cerebrospinal fluid neurochemical pattern in Menkes diseaseS G Kaler, D S Goldstein, C Holmes, et al.

Clinical Genetics|May 26, 2010

Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes diseaseV Desai, A Donsante, K J Swoboda, et al.

American Journal of Medical Genetics|April 1, 1983

Brief clinical report: two children with de novo del(9p)R S Young, P Bader, C G Palmer, et al.

Genetic Testing|August 23, 2000

Novel method for molecular detection of the two common hereditary hemochromatosis mutationsS G Kaler, J M Devaney, E L Pettit, et al.

British Medical Bulletin|April 1, 1993

Travel vaccines--a review of current thinkingJ H Levin, P D Clarke

American Journal of Medical Genetics|October 2, 1996

Distinctive Menkes disease variant with occipital horns: delineation of natural history and clinical phenotypeV K Proud, H G Mussell, S G Kaler, et al.

Pediatric Research|February 1, 1994

Metallothionein synthesis and degradation in Indian childhood cirrhosis fibroblastsS H Hahn, M L Brantly, C Oliver, et al.

Fertility and Sterility|October 1, 1991

Is the inappropriate gonadotropin secretion of patients with polycystic ovary syndrome similar to that of patients with adult-onset congenital adrenal hyperplasia?J H Levin, E Carmina, R A Lobo

Analytical Chemistry|February 24, 2001

Genotyping of two mutations in the HFE gene using single-base extension and high-performance liquid chromatographyJ M Devaney, E L Pettit, S G Kaler, et al.

Pageof 4