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M Golabi

Showing results (31-40 of 53) with videos related to

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Clinical Genetics|March 21, 2002
Tandem duplication mosaicism: characterization of a mosaic dup(5q) and reviewK A Rauen, S M Bitts, L Li, et al.
American Journal of Medical Genetics|May 26, 1999
Gastrointestinal tract anomalies in velocardiofacial syndromeG M Enns, V A Cox, M Golabi, et al.
American Journal of Medical Genetics|August 5, 2000
Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndromeK A Rauen, P D Cotter, S M Bitts, et al.
American Journal of Medical Genetics|September 11, 1992
Beare-Stevenson cutis gyrata syndromeB D Hall, R G Cadle, M Golabi, et al.
Journal of Enzyme Inhibition|October 13, 2000
Nickel-induced substrate inhibition of bovine liver glutamate dehydrogenaseS Ghobadi, M Nemat-Gorgani, S M Golabi, et al.
American Journal of Medical Genetics|December 18, 1998
Severe congenital anomalies requiring transplantation in children with Kabuki syndromeA Ewart-Toland, G M Enns, V A Cox, et al.
Neurology|August 1, 1985
Emery-Dreifuss muscular dystrophy with autosomal dominant transmissionR G Miller, R B Layzer, M A Mellenthin, et al.
American Journal of Medical Genetics|October 27, 1998
Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature reviewG M Enns, V A Cox, R B Goldstein, et al.
American Journal of Medical Genetics|March 10, 2000
Oculoauriculovertebral abnormalities in children of diabetic mothersA Ewart-Toland, J Yankowitz, A Winder, et al.
American Journal of Medical Genetics|September 14, 1999
Apparent cyclophosphamide (cytoxan) embryopathy: a distinct phenotype?G M Enns, E Roeder, R T Chan, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Clinical Genetics|March 21, 2002
Tandem duplication mosaicism: characterization of a mosaic dup(5q) and reviewK A Rauen, S M Bitts, L Li, et al.
American Journal of Medical Genetics|May 26, 1999
Gastrointestinal tract anomalies in velocardiofacial syndromeG M Enns, V A Cox, M Golabi, et al.
American Journal of Medical Genetics|August 5, 2000
Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndromeK A Rauen, P D Cotter, S M Bitts, et al.
American Journal of Medical Genetics|September 11, 1992
Beare-Stevenson cutis gyrata syndromeB D Hall, R G Cadle, M Golabi, et al.
Journal of Enzyme Inhibition|October 13, 2000
Nickel-induced substrate inhibition of bovine liver glutamate dehydrogenaseS Ghobadi, M Nemat-Gorgani, S M Golabi, et al.
American Journal of Medical Genetics|December 18, 1998
Severe congenital anomalies requiring transplantation in children with Kabuki syndromeA Ewart-Toland, G M Enns, V A Cox, et al.
Neurology|August 1, 1985
Emery-Dreifuss muscular dystrophy with autosomal dominant transmissionR G Miller, R B Layzer, M A Mellenthin, et al.
American Journal of Medical Genetics|October 27, 1998
Congenital diaphragmatic defects and associated syndromes, malformations, and chromosome anomalies: a retrospective study of 60 patients and literature reviewG M Enns, V A Cox, R B Goldstein, et al.
American Journal of Medical Genetics|March 10, 2000
Oculoauriculovertebral abnormalities in children of diabetic mothersA Ewart-Toland, J Yankowitz, A Winder, et al.
American Journal of Medical Genetics|September 14, 1999
Apparent cyclophosphamide (cytoxan) embryopathy: a distinct phenotype?G M Enns, E Roeder, R T Chan, et al.
Pageof 6