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Clinical Genetics
|
October 12, 2001
Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features
C Orellana, F Martínez, L Badía, et al.
Cancer Genetics and Cytogenetics
|
August 1, 1995
Renal adenocarcinoma in an 8-year-old child, with a t(X;17)(p11.2;q25)
M J Hernandez-Martí, C Orellana-Alonso, L Badía-Garrabou, et al.
Anales Espanoles De Pediatria
|
March 1, 1976
[Chromosome delection point in "cri du chat" syndrome (author's transl)]
F Prieto García, L Badía Garrabou, G Abeledo Mezquita, et al.
Clinical Genetics
|
August 31, 1999
Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain
J M Millán, F Martínez, A Cadroy, et al.
Medicina Clinica
|
May 5, 1990
[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]
F Palau, J J Vílchez, M Beneyto, et al.
Cytogenetic and Genome Research
|
February 18, 2006
Recombinant X chromosome in a prenatal diagnosis
C Orellana, L Badía, F Martínez, et al.
Cancer Genetics and Cytogenetics
|
April 18, 1998
Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutations
C Orellana, M Hernandez-Martí, F Martínez, et al.
Dalton Transactions (Cambridge, England : 2003)
|
June 10, 2014
Magnetic relaxation versus 3D long-range ordering in {Dy₂Ba(α-fur)₈}n furoate polymers
E Bartolomé, J Bartolomé, S Melnic, et al.
Dalton Transactions (Cambridge, England : 2003)
|
July 21, 2015
Correction: magnetic relaxation versus 3D long-range ordering in {Dy2Ba(α-fur)8}n furoate polymers
E Bartolomé, J Bartolomé, S Melnic, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Clinical Genetics
|
October 12, 2001
Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features
C Orellana, F Martínez, L Badía, et al.
Cancer Genetics and Cytogenetics
|
August 1, 1995
Renal adenocarcinoma in an 8-year-old child, with a t(X;17)(p11.2;q25)
M J Hernandez-Martí, C Orellana-Alonso, L Badía-Garrabou, et al.
Anales Espanoles De Pediatria
|
March 1, 1976
[Chromosome delection point in "cri du chat" syndrome (author's transl)]
F Prieto García, L Badía Garrabou, G Abeledo Mezquita, et al.
Clinical Genetics
|
August 31, 1999
Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain
J M Millán, F Martínez, A Cadroy, et al.
Medicina Clinica
|
May 5, 1990
[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]
F Palau, J J Vílchez, M Beneyto, et al.
Cytogenetic and Genome Research
|
February 18, 2006
Recombinant X chromosome in a prenatal diagnosis
C Orellana, L Badía, F Martínez, et al.
Cancer Genetics and Cytogenetics
|
April 18, 1998
Pediatric brain tumors: loss of heterozygosity at 17p and TP53 gene mutations
C Orellana, M Hernandez-Martí, F Martínez, et al.
Dalton Transactions (Cambridge, England : 2003)
|
June 10, 2014
Magnetic relaxation versus 3D long-range ordering in {Dy₂Ba(α-fur)₈}n furoate polymers
E Bartolomé, J Bartolomé, S Melnic, et al.
Dalton Transactions (Cambridge, England : 2003)
|
July 21, 2015
Correction: magnetic relaxation versus 3D long-range ordering in {Dy2Ba(α-fur)8}n furoate polymers
E Bartolomé, J Bartolomé, S Melnic, et al.
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of 3