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Journal of Child Neurology
|
November 1, 1995
Seizure and EEG patterns in Angelman's syndrome
F Viani, A Romeo, M Viri, et al.
American Journal of Medical Genetics
|
November 15, 1993
Variability of the Brachmann-de Lange syndrome
A Selicorni, F Lalatta, E Livini, et al.
American Journal of Medical Genetics
|
December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment
F Lalatta, D Clerici Bagozzi, M G Salmoiraghi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 8, 2011
Double pituitary and conserved function in an adult patient with neurofibromatosis type 1
M Filopanti, U Verga, F Ermetici, et al.
American Journal of Medical Genetics
|
December 1, 1992
Limb anomalies following chorionic villus sampling: a registry based case-control study
P Mastroiacovo, L D Botto, D P Cavalcanti, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis
S Giliani, M Fiorini, P Mella, et al.
Journal of Endocrinological Investigation
|
July 22, 2018
Bone involvement and mineral metabolism in Williams' syndrome
S Palmieri, M F Bedeschi, E Cairoli, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
September 3, 2010
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene
B Gentilin, F Forzano, M F Bedeschi, et al.
Epigenetics
|
September 18, 2018
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
L Fontana, M F Bedeschi, S Maitz, et al.
Minerva Pediatrica
|
October 1, 1996
The Williams syndrome: an Italian collaborative study
P Franceschini, A Guala, M P Vardeu, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Journal of Child Neurology
|
November 1, 1995
Seizure and EEG patterns in Angelman's syndrome
F Viani, A Romeo, M Viri, et al.
American Journal of Medical Genetics
|
November 15, 1993
Variability of the Brachmann-de Lange syndrome
A Selicorni, F Lalatta, E Livini, et al.
American Journal of Medical Genetics
|
December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment
F Lalatta, D Clerici Bagozzi, M G Salmoiraghi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 8, 2011
Double pituitary and conserved function in an adult patient with neurofibromatosis type 1
M Filopanti, U Verga, F Ermetici, et al.
American Journal of Medical Genetics
|
December 1, 1992
Limb anomalies following chorionic villus sampling: a registry based case-control study
P Mastroiacovo, L D Botto, D P Cavalcanti, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis
S Giliani, M Fiorini, P Mella, et al.
Journal of Endocrinological Investigation
|
July 22, 2018
Bone involvement and mineral metabolism in Williams' syndrome
S Palmieri, M F Bedeschi, E Cairoli, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
September 3, 2010
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene
B Gentilin, F Forzano, M F Bedeschi, et al.
Epigenetics
|
September 18, 2018
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders
L Fontana, M F Bedeschi, S Maitz, et al.
Minerva Pediatrica
|
October 1, 1996
The Williams syndrome: an Italian collaborative study
P Franceschini, A Guala, M P Vardeu, et al.
Page
of 5