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Ars Curandi Em Odontologia
|
May 1, 1976
[Treatment by the dentist of the newborn with cleft lip and palate]
A Pezzolo
Annales De Genetique
|
January 1, 1994
Maternal derivation of inv dup (22) and clinical variation in cat-eye syndrome
R Tupler, A Hoeller, A Pezzolo, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Molecular and cytogenetic characterization of radiation hybrids specific for human chromosome 16
I Ceccherini, A Pezzolo, P Persici, et al.
Minerva Medica
|
January 7, 1998
[Prenatal diagnosis of triploidy and trisomy 21 through fetal erythroblasts isolated from maternal blood]
A Pezzolo, F Santi, V Pistoia, et al.
Prenatal Diagnosis
|
April 1, 1997
Prenatal diagnosis of triploidy using fetal cells in the maternal circulation
A Pezzolo, F Santi, V Pistoia, et al.
Journal of Medical Genetics
|
May 1, 1993
ICF syndrome with variable expression in sibs
G Gimelli, P Varone, A Pezzolo, et al.
Prenatal Diagnosis
|
August 1, 1990
Prenatal diagnosis of a partial 8p trisomy
A Pezzolo, M P Bicocchi, C Zampatti, et al.
Human Genetics
|
February 1, 1994
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2
A Pezzolo, G Gimelli, M Sposito, et al.
Clinical Genetics
|
January 1, 1996
The phenotype of a 45,X male with a Y/18 translocation
G Gimelli, R Cinti, P Varone, et al.
Human Genetics
|
March 1, 1993
Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?
G M Ghiggeri, G Caridi, P Altieri, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Ars Curandi Em Odontologia
|
May 1, 1976
[Treatment by the dentist of the newborn with cleft lip and palate]
A Pezzolo
Annales De Genetique
|
January 1, 1994
Maternal derivation of inv dup (22) and clinical variation in cat-eye syndrome
R Tupler, A Hoeller, A Pezzolo, et al.
Cytogenetics and Cell Genetics
|
January 1, 1992
Molecular and cytogenetic characterization of radiation hybrids specific for human chromosome 16
I Ceccherini, A Pezzolo, P Persici, et al.
Minerva Medica
|
January 7, 1998
[Prenatal diagnosis of triploidy and trisomy 21 through fetal erythroblasts isolated from maternal blood]
A Pezzolo, F Santi, V Pistoia, et al.
Prenatal Diagnosis
|
April 1, 1997
Prenatal diagnosis of triploidy using fetal cells in the maternal circulation
A Pezzolo, F Santi, V Pistoia, et al.
Journal of Medical Genetics
|
May 1, 1993
ICF syndrome with variable expression in sibs
G Gimelli, P Varone, A Pezzolo, et al.
Prenatal Diagnosis
|
August 1, 1990
Prenatal diagnosis of a partial 8p trisomy
A Pezzolo, M P Bicocchi, C Zampatti, et al.
Human Genetics
|
February 1, 1994
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2
A Pezzolo, G Gimelli, M Sposito, et al.
Clinical Genetics
|
January 1, 1996
The phenotype of a 45,X male with a Y/18 translocation
G Gimelli, R Cinti, P Varone, et al.
Human Genetics
|
March 1, 1993
Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?
G M Ghiggeri, G Caridi, P Altieri, et al.
Page
of 3