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American Journal of Medical Genetics. Part A
|
March 23, 2005
Renpenning syndrome comes into focus
Roger E Stevenson, C W Bennett, F Abidi, et al.
Cytogenetic and Genome Research
|
November 9, 2005
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies
S S Bhat, K R Schmidt, S Ladd, et al.
American Journal of Medical Genetics
|
September 1, 1994
Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome
R E Stevenson, M May, J F Arena, et al.
Journal of Autism and Developmental Disorders
|
October 20, 2000
The HOPA gene dodecamer duplication is not a significant etiological factor in autism
R C Michaelis, S A Copeland-Yates, K Sossey-Alaoui, et al.
Clinical Genetics
|
November 17, 2007
Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism
S S Bhat, S Ladd, F Grass, et al.
American Journal of Medical Genetics
|
February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter study
G S Fisch, T Arinami, U Froster-Iskenius, et al.
American Journal of Medical Genetics
|
April 17, 1998
Autism and maternally derived aberrations of chromosome 15q
R J Schroer, M C Phelan, R C Michaelis, et al.
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of 3
Search research articles
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Showing results (21-30 of 27) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 27 results.
American Journal of Medical Genetics. Part A
|
March 23, 2005
Renpenning syndrome comes into focus
Roger E Stevenson, C W Bennett, F Abidi, et al.
Cytogenetic and Genome Research
|
November 9, 2005
Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies
S S Bhat, K R Schmidt, S Ladd, et al.
American Journal of Medical Genetics
|
September 1, 1994
Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome
R E Stevenson, M May, J F Arena, et al.
Journal of Autism and Developmental Disorders
|
October 20, 2000
The HOPA gene dodecamer duplication is not a significant etiological factor in autism
R C Michaelis, S A Copeland-Yates, K Sossey-Alaoui, et al.
Clinical Genetics
|
November 17, 2007
Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism
S S Bhat, S Ladd, F Grass, et al.
American Journal of Medical Genetics
|
February 1, 1991
Relationship between age and IQ among fragile X males: a multicenter study
G S Fisch, T Arinami, U Froster-Iskenius, et al.
American Journal of Medical Genetics
|
April 17, 1998
Autism and maternally derived aberrations of chromosome 15q
R J Schroer, M C Phelan, R C Michaelis, et al.
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of 3