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American Journal of Medical Genetics
|
December 20, 2000
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH
C Goizet, E Excoffier, L Taine, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1995
Seeding of YACs over regions 1q41-q42.3 and 11q14.3-q23 with microdissection clones
J Petit, P Boisseau, K Evans, et al.
Nucleic Acids Research
|
July 11, 1986
A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h]
K Wrogemann, B Arveiler, I Oberle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 15, 2011
[Polymorphic expression of epilepsy and cognitive impairment in ring chromosome 20 syndrome]
F Villéga, H Ngayap, C Espil-Taris, et al.
European Journal of Medical Genetics
|
August 22, 2012
Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female
M J Alao, A Lalèyè, F Lalya, et al.
American Journal of Medical Genetics
|
May 1, 1988
Linkage analysis suggests at least two loci for X-linked non-specific mental retardation
B Arveiler, Y Alembik, A Hanauer, et al.
American Journal of Medical Genetics
|
July 24, 1998
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndrome
L Taine, C Goizet, Z Q Wen, et al.
Journal of Medical Genetics
|
June 19, 2002
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
I Coupry, C Roudaut, M Stef, et al.
Human Genetics
|
March 1, 1988
Multilocus analysis of the fragile X syndrome
W T Brown, A Gross, C Chan, et al.
Genomics
|
August 10, 1995
A contiguous clone map over 3 Mb on the long arm of chromosome 11 across a balanced translocation associated with schizophrenia
K L Evans, J Brown, Y Shibasaki, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 64) with videos related to
Sort By:
Page
of 7
American Journal of Medical Genetics
|
December 20, 2000
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH
C Goizet, E Excoffier, L Taine, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1995
Seeding of YACs over regions 1q41-q42.3 and 11q14.3-q23 with microdissection clones
J Petit, P Boisseau, K Evans, et al.
Nucleic Acids Research
|
July 11, 1986
A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h]
K Wrogemann, B Arveiler, I Oberle, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 15, 2011
[Polymorphic expression of epilepsy and cognitive impairment in ring chromosome 20 syndrome]
F Villéga, H Ngayap, C Espil-Taris, et al.
European Journal of Medical Genetics
|
August 22, 2012
Blepharophimosis, ptosis, epicanthus inversus syndrome with translocation and deletion at chromosome 3q23 in a black African female
M J Alao, A Lalèyè, F Lalya, et al.
American Journal of Medical Genetics
|
May 1, 1988
Linkage analysis suggests at least two loci for X-linked non-specific mental retardation
B Arveiler, Y Alembik, A Hanauer, et al.
American Journal of Medical Genetics
|
July 24, 1998
Submicroscopic deletion of chromosome 16p13.3 in patients with Rubinstein-Taybi syndrome
L Taine, C Goizet, Z Q Wen, et al.
Journal of Medical Genetics
|
June 19, 2002
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
I Coupry, C Roudaut, M Stef, et al.
Human Genetics
|
March 1, 1988
Multilocus analysis of the fragile X syndrome
W T Brown, A Gross, C Chan, et al.
Genomics
|
August 10, 1995
A contiguous clone map over 3 Mb on the long arm of chromosome 11 across a balanced translocation associated with schizophrenia
K L Evans, J Brown, Y Shibasaki, et al.
Page
of 7