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M G BUTLER

Showing results (141-150 of 165) with videos related to

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American Journal of Medical Genetics|February 1, 1991
Anthropometric comparison of mentally retarded males with and without the fragile X syndromeM G Butler, G A Allen, J L Haynes, et al.
American Journal of Medical Genetics|January 1, 1988
Two patients with ring chromosome 15 syndromeM G Butler, A B Fogo, D A Fuchs, et al.
Journal of Intellectual Disability Research : JIDR|December 1, 2005
A measure of food seeking in individuals with Prader-Willi syndromeJ Young, J Zarcone, L Holsen, et al.
Regulatory Peptides|September 1, 1983
Distribution and characterisation of immunoreactive somatostatin in human gastrointestinal tractE Penman, J A Wass, M G Butler, et al.
American Journal of Medical Genetics|December 1, 1988
Metacarpophalangeal pattern profile analysis in fragile X syndromeM G Butler, M Fletcher, D D Gale, et al.
Journal of Intellectual Disability Research : JIDR|May 12, 2007
The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndromeJ Zarcone, D Napolitano, C Peterson, et al.
Clinical Dysmorphology|April 20, 2001
Total anomalous pulmonary venous connection and a constellation of craniofacial, skeletal, and urogenital anomalies in a newborn and similar features in his 36-year-old fatherD M Pierson, E M Taboada, G K Lofland, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Pediatrics|February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteriaV A Holm, S B Cassidy, M G Butler, et al.
American Journal of Medical Genetics|March 21, 1998
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qG H Vance, C Nickerson, L Sarnat, et al.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics|February 1, 1991
Anthropometric comparison of mentally retarded males with and without the fragile X syndromeM G Butler, G A Allen, J L Haynes, et al.
American Journal of Medical Genetics|January 1, 1988
Two patients with ring chromosome 15 syndromeM G Butler, A B Fogo, D A Fuchs, et al.
Journal of Intellectual Disability Research : JIDR|December 1, 2005
A measure of food seeking in individuals with Prader-Willi syndromeJ Young, J Zarcone, L Holsen, et al.
Regulatory Peptides|September 1, 1983
Distribution and characterisation of immunoreactive somatostatin in human gastrointestinal tractE Penman, J A Wass, M G Butler, et al.
American Journal of Medical Genetics|December 1, 1988
Metacarpophalangeal pattern profile analysis in fragile X syndromeM G Butler, M Fletcher, D D Gale, et al.
Journal of Intellectual Disability Research : JIDR|May 12, 2007
The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndromeJ Zarcone, D Napolitano, C Peterson, et al.
Clinical Dysmorphology|April 20, 2001
Total anomalous pulmonary venous connection and a constellation of craniofacial, skeletal, and urogenital anomalies in a newborn and similar features in his 36-year-old fatherD M Pierson, E M Taboada, G K Lofland, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Pediatrics|February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteriaV A Holm, S B Cassidy, M G Butler, et al.
American Journal of Medical Genetics|March 21, 1998
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7qG H Vance, C Nickerson, L Sarnat, et al.
Pageof 17