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Pathologica
|
May 1, 1979
[Trisomy 10p due to t(Y;10)(p11; p11) "de novo"]
L Chessa, P Vignetti, E Ferrante, et al.
Journal of Medical Genetics
|
April 1, 1993
Coarctation of the aorta, interrupted aortic arch, and hypoplastic left heart syndrome in three generations
S Gerboni, G Sabatino, R Mingarelli, et al.
American Journal of Medical Genetics
|
August 1, 1989
Autosomal recessive form of whistling face syndrome in sibs
B Dallapiccola, A Giannotti, A Lembo, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1994
The up-to-date molecular genetics of cystic fibrosis
G Novelli, F Sangiuolo, P Maceratesi, et al.
Acta Haematologica
|
January 1, 1984
Increased activity of glutathione S-transferase and fast decay of reduced glutathione in Fanconi's anemia erythrocytes
B Dallapiccola, M Magnani, G Novelli, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1997
From genetic research into clinical practice
B Dallapiccola, I Torrente, R Mingarelli, et al.
Prenatal Diagnosis
|
May 1, 1987
First trimester studies of a fetus at risk for triose phosphate isomerase deficiency
B Dallapiccola, G Novelli, C Cuoco, et al.
Gene Therapy
|
May 29, 2002
Extrachromosomal genes: a powerful tool in gene targeting approaches
A Colosimo, V Guida, G Palka, et al.
Hereditas
|
January 1, 1980
Aberrations of chromosome No. 1 in blastic phase of chronic myeloid leukemia
G Alimena, B Dallapiccola, F Mitelman, et al.
Human Genetics
|
July 7, 1976
Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome
B Dallapiccola, G Bollea, C Mazzilli, et al.
Page
of 48
Search research articles
Search
Showing results (81-90 of 479) with videos related to
Sort By:
Page
of 48
Pathologica
|
May 1, 1979
[Trisomy 10p due to t(Y;10)(p11; p11) "de novo"]
L Chessa, P Vignetti, E Ferrante, et al.
Journal of Medical Genetics
|
April 1, 1993
Coarctation of the aorta, interrupted aortic arch, and hypoplastic left heart syndrome in three generations
S Gerboni, G Sabatino, R Mingarelli, et al.
American Journal of Medical Genetics
|
August 1, 1989
Autosomal recessive form of whistling face syndrome in sibs
B Dallapiccola, A Giannotti, A Lembo, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|
January 1, 1994
The up-to-date molecular genetics of cystic fibrosis
G Novelli, F Sangiuolo, P Maceratesi, et al.
Acta Haematologica
|
January 1, 1984
Increased activity of glutathione S-transferase and fast decay of reduced glutathione in Fanconi's anemia erythrocytes
B Dallapiccola, M Magnani, G Novelli, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1997
From genetic research into clinical practice
B Dallapiccola, I Torrente, R Mingarelli, et al.
Prenatal Diagnosis
|
May 1, 1987
First trimester studies of a fetus at risk for triose phosphate isomerase deficiency
B Dallapiccola, G Novelli, C Cuoco, et al.
Gene Therapy
|
May 29, 2002
Extrachromosomal genes: a powerful tool in gene targeting approaches
A Colosimo, V Guida, G Palka, et al.
Hereditas
|
January 1, 1980
Aberrations of chromosome No. 1 in blastic phase of chronic myeloid leukemia
G Alimena, B Dallapiccola, F Mitelman, et al.
Human Genetics
|
July 7, 1976
Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome
B Dallapiccola, G Bollea, C Mazzilli, et al.
Page
of 48