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Acta Neurologica
|
November 1, 1977
[Complicated spastic paraplegia with sex-linked inheritance (report of a family)]
G Galassi, A Penne, A Colombo, et al.
Brain & Development
|
January 1, 1990
Molecular analysis of the Rett syndrome using cDNA synapsin I as a probe
A Ferlini, L Ansaloni, C Nobile, et al.
Minerva Pediatrica
|
September 15, 1973
[Familial t (22q Dq) translocation and free trisomy 21 in offspring]
A Forabosco, E Cheli, L Marzona, et al.
Lancet (London, England)
|
August 5, 1978
H-Y antigen in a male with 45, X karyotype
A Forabosco, E Cheli, B Noel, et al.
Annales De Genetique
|
December 1, 1972
[Ring 15 chromosome: r(15). Identification by controlled denaturation]
A Forabosco, B Dutrillaux, G Vassoler, et al.
Helvetica Paediatrica Acta
|
October 1, 1975
Trisomy of the distal third of the long arm of chromosome 10. Report of a new case due to a familial translocation t(10;18) (q24;p11)
A Forabosco, S Bernasconi, G Giovannelli, et al.
American Journal of Medical Genetics
|
July 1, 1990
Distal 12p deletion in a stillborn infant
A Baroncini, C Avellini, C Neri, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1973
Skeletal changes in the "cri du chat" syndrome
B Dallapiccola, G Pistocchi, A Forabosco, et al.
European Journal of Pediatrics
|
April 1, 1990
Ring chromosome 7: report of the fifth case
G M Caramia, A Baroncini, P Osimani, et al.
Anatomy and Embryology
|
February 7, 1998
Emx2 developmental expression in the primordia of the reproductive and excretory systems
M Pellegrini, S Pantano, F Lucchini, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 134) with videos related to
Sort By:
Page
of 14
Acta Neurologica
|
November 1, 1977
[Complicated spastic paraplegia with sex-linked inheritance (report of a family)]
G Galassi, A Penne, A Colombo, et al.
Brain & Development
|
January 1, 1990
Molecular analysis of the Rett syndrome using cDNA synapsin I as a probe
A Ferlini, L Ansaloni, C Nobile, et al.
Minerva Pediatrica
|
September 15, 1973
[Familial t (22q Dq) translocation and free trisomy 21 in offspring]
A Forabosco, E Cheli, L Marzona, et al.
Lancet (London, England)
|
August 5, 1978
H-Y antigen in a male with 45, X karyotype
A Forabosco, E Cheli, B Noel, et al.
Annales De Genetique
|
December 1, 1972
[Ring 15 chromosome: r(15). Identification by controlled denaturation]
A Forabosco, B Dutrillaux, G Vassoler, et al.
Helvetica Paediatrica Acta
|
October 1, 1975
Trisomy of the distal third of the long arm of chromosome 10. Report of a new case due to a familial translocation t(10;18) (q24;p11)
A Forabosco, S Bernasconi, G Giovannelli, et al.
American Journal of Medical Genetics
|
July 1, 1990
Distal 12p deletion in a stillborn infant
A Baroncini, C Avellini, C Neri, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1973
Skeletal changes in the "cri du chat" syndrome
B Dallapiccola, G Pistocchi, A Forabosco, et al.
European Journal of Pediatrics
|
April 1, 1990
Ring chromosome 7: report of the fifth case
G M Caramia, A Baroncini, P Osimani, et al.
Anatomy and Embryology
|
February 7, 1998
Emx2 developmental expression in the primordia of the reproductive and excretory systems
M Pellegrini, S Pantano, F Lucchini, et al.
Page
of 14