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Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1975
Leucocyte morphology and chromosome morphology
B Dallapiccola, O Baricordi, L Capra, et al.
Journal of Medical Genetics
|
October 1, 1982
"Microcytogenetics" and Langer-Giedion syndrome
M Frontali, M Ramenghi, S Trabace, et al.
Annales De Genetique
|
January 1, 1980
Identification of the origin of a 22p+ chromosome by triplex dosage effect of LDH B, GAPHD, TPI and ENO2
B Dallapiccola, V Brinchi, M Magnani, et al.
Prenatal Diagnosis
|
September 1, 1984
Prenatal diagnosis of recurrence of cystic hygroma with normal chromosomes
B Dallapiccola, L Zelante, G Perla, et al.
Annales De Genetique
|
January 1, 1991
Ring chromosome 8 associated with microcephaly
R Mingarelli, G Valorani, L Zelante, et al.
Genomics
|
April 1, 1991
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis
F Sangiuolo, G Novelli, S Murru, et al.
American Journal of Medical Genetics
|
February 15, 1993
Confirmation of the mandibulofacial dysostosis, Toriello type
L Zelante, L Vigliaroli, R Mingarelli, et al.
Human Genetics
|
September 1, 1979
Confirmation of regional assignment of nucleoside phosphorylase to band 14q13 by gene-dosage studies
B Dallapiccola, M Magnani, M Dachà, et al.
Journal of Mental Deficiency Research
|
December 1, 1980
Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities
M Zannotti, A Preto, P R Giovanardi, et al.
Journal of Medical Genetics
|
December 1, 1996
Heterotaxia syndromes and 22q11 deletion
B Marino, M C Digilio, A Giannotti, et al.
Page
of 48
Search research articles
Search
Showing results (111-120 of 479) with videos related to
Sort By:
Page
of 48
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1975
Leucocyte morphology and chromosome morphology
B Dallapiccola, O Baricordi, L Capra, et al.
Journal of Medical Genetics
|
October 1, 1982
"Microcytogenetics" and Langer-Giedion syndrome
M Frontali, M Ramenghi, S Trabace, et al.
Annales De Genetique
|
January 1, 1980
Identification of the origin of a 22p+ chromosome by triplex dosage effect of LDH B, GAPHD, TPI and ENO2
B Dallapiccola, V Brinchi, M Magnani, et al.
Prenatal Diagnosis
|
September 1, 1984
Prenatal diagnosis of recurrence of cystic hygroma with normal chromosomes
B Dallapiccola, L Zelante, G Perla, et al.
Annales De Genetique
|
January 1, 1991
Ring chromosome 8 associated with microcephaly
R Mingarelli, G Valorani, L Zelante, et al.
Genomics
|
April 1, 1991
A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis
F Sangiuolo, G Novelli, S Murru, et al.
American Journal of Medical Genetics
|
February 15, 1993
Confirmation of the mandibulofacial dysostosis, Toriello type
L Zelante, L Vigliaroli, R Mingarelli, et al.
Human Genetics
|
September 1, 1979
Confirmation of regional assignment of nucleoside phosphorylase to band 14q13 by gene-dosage studies
B Dallapiccola, M Magnani, M Dachà, et al.
Journal of Mental Deficiency Research
|
December 1, 1980
Extra dicentric 15 pter leads to q21/22 chromosomes in five unrelated patients with a distinct syndrome of progressive psychomotor retardation, seizures, hyper-reactivity and dermatoglyphic abnormalities
M Zannotti, A Preto, P R Giovanardi, et al.
Journal of Medical Genetics
|
December 1, 1996
Heterotaxia syndromes and 22q11 deletion
B Marino, M C Digilio, A Giannotti, et al.
Page
of 48