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American Journal of Medical Genetics
|
March 13, 1995
Further case of trisomy 18 mosaicism with a mild phenotype
A L Collins, J Fisher, J A Crolla, et al.
Singapore Medical Journal
|
April 18, 2008
Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis
L A Gole, J Lim, J A Crolla, et al.
Nature
|
March 22, 1979
Meiotic crossing over exchange in the female mouse visualised by BUdR substitution
P E Polani, J A Crolla, M J Seller, et al.
Journal of Medical Genetics
|
February 24, 2001
An analphoid supernumerary marker chromosome derived from chromosome 3 ascertained in a fetus with multiple malformations
A E Cockwell, B Gibbons, I E Moore, et al.
American Journal of Medical Genetics
|
July 9, 1999
Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break
H Rivera, A I Vasquez, D García-Cruz, et al.
Cancer Genetics and Cytogenetics
|
May 22, 1998
Origin of the mar3 in the myeloid cell line HL-60 determined by fluorescence in situ hybridization
S H Birdsall, A McManus, J M Shipley, et al.
Journal of Medical Genetics
|
January 1, 1991
An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes
C Cooper, J A Crolla, C Laister, et al.
Journal of Medical Genetics
|
January 1, 1996
FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13)
J A Crolla, I Cross, N Atkey, et al.
Clinical Genetics
|
January 1, 1976
A three chromosome translocation involving two homologous chromosomes in a trisomic abortus
M R Creasy, J A Crolla, P E Polani, et al.
American Journal of Medical Genetics
|
December 18, 2001
FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation
A E Cockwell, I P Dávalos, H R Rivera, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 78) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics
|
March 13, 1995
Further case of trisomy 18 mosaicism with a mild phenotype
A L Collins, J Fisher, J A Crolla, et al.
Singapore Medical Journal
|
April 18, 2008
Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis
L A Gole, J Lim, J A Crolla, et al.
Nature
|
March 22, 1979
Meiotic crossing over exchange in the female mouse visualised by BUdR substitution
P E Polani, J A Crolla, M J Seller, et al.
Journal of Medical Genetics
|
February 24, 2001
An analphoid supernumerary marker chromosome derived from chromosome 3 ascertained in a fetus with multiple malformations
A E Cockwell, B Gibbons, I E Moore, et al.
American Journal of Medical Genetics
|
July 9, 1999
Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break
H Rivera, A I Vasquez, D García-Cruz, et al.
Cancer Genetics and Cytogenetics
|
May 22, 1998
Origin of the mar3 in the myeloid cell line HL-60 determined by fluorescence in situ hybridization
S H Birdsall, A McManus, J M Shipley, et al.
Journal of Medical Genetics
|
January 1, 1991
An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes
C Cooper, J A Crolla, C Laister, et al.
Journal of Medical Genetics
|
January 1, 1996
FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13)
J A Crolla, I Cross, N Atkey, et al.
Clinical Genetics
|
January 1, 1976
A three chromosome translocation involving two homologous chromosomes in a trisomic abortus
M R Creasy, J A Crolla, P E Polani, et al.
American Journal of Medical Genetics
|
December 18, 2001
FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation
A E Cockwell, I P Dávalos, H R Rivera, et al.
Page
of 8