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American Journal of Medical Genetics
|
February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease
A Plaja, T Vendrell, D Smeets, et al.
Human Mutation
|
April 24, 2001
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications
J Alonso, P García-Miguel, J Abelairas, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 12, 2003
[Bone age delay and hypoplastic thumbs in a five year-old boy]
P Soler Palacín, D Panadès Mas, R Porcel Rubio, et al.
Journal of Medical Genetics
|
October 4, 2002
Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A gene
L Palenzuela, C Vives-Bauza, I Fernández-Cadenas, et al.
Annales De Genetique
|
January 1, 1994
Terminal deletion of 6p: report of a new case
A Plaja, R Vidal, D Soriano, et al.
Annales De Genetique
|
January 1, 1985
A case of male pseudohermaphroditism with normal androgen receptor binding and 47,XYY karyotype
J M Bosch-Banyeras, L Audi, E Sarret, et al.
Human Mutation
|
April 24, 2001
Five novel single nucleotide polymorphisms of the RB1 gene (g.5625T>C, g.70169T>G, g.76875A>T, g.78026delA, and g.150072T>C) in retinoblastoma patients
J Alonso, C Moreno, A López, et al.
Journal of Medical Genetics
|
October 3, 1999
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR
R Valero, G Marfany, R Gil-Benso, et al.
Acta Obstetrica Y Ginecologica Hispano-Lusitana
|
April 1, 1977
[Considerations on the genetic study of amniotic fluid cells]
M Muxí, J Prats, J Xercavins, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
American Journal of Medical Genetics
|
February 13, 2001
Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease
A Plaja, T Vendrell, D Smeets, et al.
Human Mutation
|
April 24, 2001
Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications
J Alonso, P García-Miguel, J Abelairas, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
March 12, 2003
[Bone age delay and hypoplastic thumbs in a five year-old boy]
P Soler Palacín, D Panadès Mas, R Porcel Rubio, et al.
Journal of Medical Genetics
|
October 4, 2002
Familial expansile osteolysis in a large Spanish kindred resulting from an insertion mutation in the TNFRSF11A gene
L Palenzuela, C Vives-Bauza, I Fernández-Cadenas, et al.
Annales De Genetique
|
January 1, 1994
Terminal deletion of 6p: report of a new case
A Plaja, R Vidal, D Soriano, et al.
Annales De Genetique
|
January 1, 1985
A case of male pseudohermaphroditism with normal androgen receptor binding and 47,XYY karyotype
J M Bosch-Banyeras, L Audi, E Sarret, et al.
Human Mutation
|
April 24, 2001
Five novel single nucleotide polymorphisms of the RB1 gene (g.5625T>C, g.70169T>G, g.76875A>T, g.78026delA, and g.150072T>C) in retinoblastoma patients
J Alonso, C Moreno, A López, et al.
Journal of Medical Genetics
|
October 3, 1999
Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR
R Valero, G Marfany, R Gil-Benso, et al.
Acta Obstetrica Y Ginecologica Hispano-Lusitana
|
April 1, 1977
[Considerations on the genetic study of amniotic fluid cells]
M Muxí, J Prats, J Xercavins, et al.
Page
of 2