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Italian Journal of Pediatrics
|
March 9, 2010
Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation
Grazia Taddeucci, Alice Bonuccelli, Ilaria Mantellassi, et al.
Fertility and Sterility
|
March 29, 2008
Ring chromosome 21 and reproductive pattern: a familial case and review of the literature
Veronica Bertini, Angelo Valetto, Angela Uccelli, et al.
Surgical Laparoscopy, Endoscopy & Percutaneous Techniques
|
June 23, 2009
Laparoscopic intestinal derotation: original technique
Mario Valle, Orietta Federici, Enrico Tarantino, et al.
International Journal of Surgery Case Reports
|
November 19, 2013
Management of Spigelian hernia caused by necrobiotic fibroma of the uterus in a pregnant woman
Radwan Kassir, Enrico Tarantino, Robert Lacheze, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2008
Molecular cytogenetic characterization of a de novo mosaic supernumerary ring chromosome 7: report of a new patient
Veronica Bertini, Angelo Valetto, Angela Uccelli, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2006
Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters: the Chudley-McCullough syndrome
Fabio Matteucci, Enrico Tarantino, Maria Cristina Bianchi, et al.
Human Mutation
|
December 24, 2002
Two cases of misinterpretation of molecular results in incontinentia pigmenti, and a PCR-based method to discriminate NEMO/IKKgamma dene deletion
Tiziana Bardaro, Geppino Falco, Angela Sparago, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
July 23, 2014
Acute acalculous cholecystitis, a rare complication of Epstein-Barr virus primary infection: report of two cases and review
Amandine Gagneux-Brunon, Florence Suy, Anne Pouvaret, et al.
Human Mutation
|
October 2, 2004
Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles
Maria Savino, Maria d'Apolito, Vincenza Formica, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2005
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate
Michele Rubini, Roberto Brusati, Giovanna Garattini, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Italian Journal of Pediatrics
|
March 9, 2010
Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation
Grazia Taddeucci, Alice Bonuccelli, Ilaria Mantellassi, et al.
Fertility and Sterility
|
March 29, 2008
Ring chromosome 21 and reproductive pattern: a familial case and review of the literature
Veronica Bertini, Angelo Valetto, Angela Uccelli, et al.
Surgical Laparoscopy, Endoscopy & Percutaneous Techniques
|
June 23, 2009
Laparoscopic intestinal derotation: original technique
Mario Valle, Orietta Federici, Enrico Tarantino, et al.
International Journal of Surgery Case Reports
|
November 19, 2013
Management of Spigelian hernia caused by necrobiotic fibroma of the uterus in a pregnant woman
Radwan Kassir, Enrico Tarantino, Robert Lacheze, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2008
Molecular cytogenetic characterization of a de novo mosaic supernumerary ring chromosome 7: report of a new patient
Veronica Bertini, Angelo Valetto, Angela Uccelli, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2006
Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters: the Chudley-McCullough syndrome
Fabio Matteucci, Enrico Tarantino, Maria Cristina Bianchi, et al.
Human Mutation
|
December 24, 2002
Two cases of misinterpretation of molecular results in incontinentia pigmenti, and a PCR-based method to discriminate NEMO/IKKgamma dene deletion
Tiziana Bardaro, Geppino Falco, Angela Sparago, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
July 23, 2014
Acute acalculous cholecystitis, a rare complication of Epstein-Barr virus primary infection: report of two cases and review
Amandine Gagneux-Brunon, Florence Suy, Anne Pouvaret, et al.
Human Mutation
|
October 2, 2004
Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles
Maria Savino, Maria d'Apolito, Vincenza Formica, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2005
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate
Michele Rubini, Roberto Brusati, Giovanna Garattini, et al.
Page
of 2