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American Journal of Medical Genetics
|
February 1, 1991
Anthropometric comparison of mentally retarded males with and without the fragile X syndrome
M G Butler, G A Allen, J L Haynes, et al.
American Journal of Medical Genetics
|
January 1, 1988
Two patients with ring chromosome 15 syndrome
M 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 syndrome
J Young, J Zarcone, L Holsen, et al.
Regulatory Peptides
|
September 1, 1983
Distribution and characterisation of immunoreactive somatostatin in human gastrointestinal tract
E Penman, J A Wass, M G Butler, et al.
American Journal of Medical Genetics
|
December 1, 1988
Metacarpophalangeal pattern profile analysis in fragile X syndrome
M 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 syndrome
J 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 father
D 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 allele
R A Spritz, T Bailin, R D Nicholls, et al.
Pediatrics
|
February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteria
V 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 7q
G H Vance, C Nickerson, L Sarnat, et al.
Page
of 17
Search research articles
Search
Showing results (141-150 of 165) with videos related to
Sort By:
Page
of 17
American Journal of Medical Genetics
|
February 1, 1991
Anthropometric comparison of mentally retarded males with and without the fragile X syndrome
M G Butler, G A Allen, J L Haynes, et al.
American Journal of Medical Genetics
|
January 1, 1988
Two patients with ring chromosome 15 syndrome
M 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 syndrome
J Young, J Zarcone, L Holsen, et al.
Regulatory Peptides
|
September 1, 1983
Distribution and characterisation of immunoreactive somatostatin in human gastrointestinal tract
E Penman, J A Wass, M G Butler, et al.
American Journal of Medical Genetics
|
December 1, 1988
Metacarpophalangeal pattern profile analysis in fragile X syndrome
M 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 syndrome
J 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 father
D 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 allele
R A Spritz, T Bailin, R D Nicholls, et al.
Pediatrics
|
February 1, 1993
Prader-Willi syndrome: consensus diagnostic criteria
V 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 7q
G H Vance, C Nickerson, L Sarnat, et al.
Page
of 17