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F Lalatta

Showing results (31-40 of 42) with videos related to

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Journal of Child Neurology|November 1, 1995
Seizure and EEG patterns in Angelman's syndromeF Viani, A Romeo, M Viri, et al.
American Journal of Medical Genetics|November 15, 1993
Variability of the Brachmann-de Lange syndromeA Selicorni, F Lalatta, E Livini, et al.
American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatmentF 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 1M 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 studyP Mastroiacovo, L D Botto, D P Cavalcanti, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.
Journal of Endocrinological Investigation|July 22, 2018
Bone involvement and mineral metabolism in Williams' syndromeS 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 geneB 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 disordersL Fontana, M F Bedeschi, S Maitz, et al.
Minerva Pediatrica|October 1, 1996
The Williams syndrome: an Italian collaborative studyP Franceschini, A Guala, M P Vardeu, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Journal of Child Neurology|November 1, 1995
Seizure and EEG patterns in Angelman's syndromeF Viani, A Romeo, M Viri, et al.
American Journal of Medical Genetics|November 15, 1993
Variability of the Brachmann-de Lange syndromeA Selicorni, F Lalatta, E Livini, et al.
American Journal of Medical Genetics|December 1, 1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatmentF 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 1M 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 studyP Mastroiacovo, L D Botto, D P Cavalcanti, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.
Journal of Endocrinological Investigation|July 22, 2018
Bone involvement and mineral metabolism in Williams' syndromeS 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 geneB 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 disordersL Fontana, M F Bedeschi, S Maitz, et al.
Minerva Pediatrica|October 1, 1996
The Williams syndrome: an Italian collaborative studyP Franceschini, A Guala, M P Vardeu, et al.
Pageof 5