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American Journal of Medical Genetics
|
February 1, 1991
Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8
W T Brown, A C Gross, P Goonewardena, et al.
Human Genetics
|
June 30, 1977
A case of 46,XY,t(1;13) (q24;q32) with mental retardation
L Wilbur, F M Curcuru-Giordano, S G Krishna, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Localization of chromosome 21 probes by in situ hybridization
W T Brown, E A Devine, S L Nolin, et al.
American Journal of Human Genetics
|
February 1, 1991
Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues
I L Cohen, V Sudhalter, A Pfadt, et al.
Journal of Autism and Developmental Disorders
|
September 1, 1982
Autism is associated with the fragile-X syndrome
W T Brown, E C Jenkins, E Friedman, et al.
European Journal of Medical Genetics
|
June 15, 2005
Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype
M Velinov, J Kupferman, H Gu, et al.
Annales De Genetique
|
June 9, 2004
Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses
M Velinov, H Gu, M Genovese, et al.
American Journal of Medical Genetics
|
April 18, 1997
Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation
C M Miezejeski, G Heaney, R Belser, et al.
American Journal of Medical Genetics
|
July 23, 1998
Normal adaptive function with learning disability in duplication 8p including band p22
S S Sklower Brooks, M Genovese, H Gu, et al.
American Journal of Medical Genetics
|
February 1, 1991
Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic villi
E C Jenkins, M M Sanz, J H Ray, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 146) with videos related to
Sort By:
Page
of 15
American Journal of Medical Genetics
|
February 1, 1991
Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8
W T Brown, A C Gross, P Goonewardena, et al.
Human Genetics
|
June 30, 1977
A case of 46,XY,t(1;13) (q24;q32) with mental retardation
L Wilbur, F M Curcuru-Giordano, S G Krishna, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Localization of chromosome 21 probes by in situ hybridization
W T Brown, E A Devine, S L Nolin, et al.
American Journal of Human Genetics
|
February 1, 1991
Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues
I L Cohen, V Sudhalter, A Pfadt, et al.
Journal of Autism and Developmental Disorders
|
September 1, 1982
Autism is associated with the fragile-X syndrome
W T Brown, E C Jenkins, E Friedman, et al.
European Journal of Medical Genetics
|
June 15, 2005
Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype
M Velinov, J Kupferman, H Gu, et al.
Annales De Genetique
|
June 9, 2004
Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses
M Velinov, H Gu, M Genovese, et al.
American Journal of Medical Genetics
|
April 18, 1997
Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation
C M Miezejeski, G Heaney, R Belser, et al.
American Journal of Medical Genetics
|
July 23, 1998
Normal adaptive function with learning disability in duplication 8p including band p22
S S Sklower Brooks, M Genovese, H Gu, et al.
American Journal of Medical Genetics
|
February 1, 1991
Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic villi
E C Jenkins, M M Sanz, J H Ray, et al.
Page
of 15