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M Silengo

Showing results (31-40 of 52) with videos related to

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Clinical Genetics|September 1, 1992
Autosomal recessive microcephaly with early onset seizures and spasticityM Silengo, M Lerone, M Martinelli, et al.
Minerva Pediatrica|October 1, 1995
[Cardiofacial syndrome. A case report]M Bado, G Morreale, M Pelegrini, et al.
Clinical Genetics|August 17, 2000
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 geneM Priolo, M Lerone, M Baffico, et al.
La Radiologia Medica|April 27, 2002
Complex cerebral malformation including Dandy-Walker in a newborn with trisomy 9 mosaicismP Murru, A Coscia, C Martano, et al.
Clinical Genetics|December 1, 1987
Postmortem Menkes diagnosis from carrier testing of female relativesT Tønnesen, M Silengo, A M Gerdes, et al.
Clinical Dysmorphology|October 25, 2000
Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?M Priolo, M Lerone, L Rosaia, et al.
Clinical Genetics|July 1, 1988
X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogeneA Ballabio, G Parenti, R Carrozzo, et al.
Pediatric Radiology|January 1, 1991
Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvementM Lerone, P Dodero, G Romeo, et al.
American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.
Oncogene|June 15, 1995
RET mutations in exons 13 and 14 of FMTC patientsA Bolino, I Schuffenecker, Y Luo, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Clinical Genetics|September 1, 1992
Autosomal recessive microcephaly with early onset seizures and spasticityM Silengo, M Lerone, M Martinelli, et al.
Minerva Pediatrica|October 1, 1995
[Cardiofacial syndrome. A case report]M Bado, G Morreale, M Pelegrini, et al.
Clinical Genetics|August 17, 2000
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 geneM Priolo, M Lerone, M Baffico, et al.
La Radiologia Medica|April 27, 2002
Complex cerebral malformation including Dandy-Walker in a newborn with trisomy 9 mosaicismP Murru, A Coscia, C Martano, et al.
Clinical Genetics|December 1, 1987
Postmortem Menkes diagnosis from carrier testing of female relativesT Tønnesen, M Silengo, A M Gerdes, et al.
Clinical Dysmorphology|October 25, 2000
Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?M Priolo, M Lerone, L Rosaia, et al.
Clinical Genetics|July 1, 1988
X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogeneA Ballabio, G Parenti, R Carrozzo, et al.
Pediatric Radiology|January 1, 1991
Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvementM Lerone, P Dodero, G Romeo, et al.
American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.
Oncogene|June 15, 1995
RET mutations in exons 13 and 14 of FMTC patientsA Bolino, I Schuffenecker, Y Luo, et al.
Pageof 6