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M C Silengo

Showing results (21-30 of 28) with videos related to

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Clinical Genetics|February 1, 1984
The Neu-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a caseM C Silengo, G Davi, R Bianco, et al.
Clinical Genetics|May 1, 1982
Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndromeM C Silengo, G F Davi, R Bianco, et al.
Clinical Genetics|June 1, 1984
Interstitial deletion of chromosome 1 (q23-q25). Report of a caseM C Silengo, G F Davi, R Bianco, et al.
American Journal of Medical Genetics|October 21, 1999
Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndromeP G Mori, M Priolo, M Lerone, et al.
Clinical Genetics|December 1, 1986
Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivityM C Silengo, G L Bell, M Biagioli, et al.
Nature Communications|March 17, 2021
Ground deformation reveals the scale-invariant conduit dynamics driving explosive basaltic eruptionsM Ripepe, G Lacanna, M Pistolesi, et al.
Clinical Genetics|February 10, 2016
Fetal growth patterns in Beckwith-Wiedemann syndromeA Mussa, S Russo, A de Crescenzo, et al.
Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Clinical Genetics|February 1, 1984
The Neu-COFS (cerebro-oculo-facio-skeletal) syndrome: report of a caseM C Silengo, G Davi, R Bianco, et al.
Clinical Genetics|May 1, 1982
Distinctive hair changes (pili torti) in Rapp-Hodgkin ectodermal dysplasia syndromeM C Silengo, G F Davi, R Bianco, et al.
Clinical Genetics|June 1, 1984
Interstitial deletion of chromosome 1 (q23-q25). Report of a caseM C Silengo, G F Davi, R Bianco, et al.
American Journal of Medical Genetics|October 21, 1999
Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndromeP G Mori, M Priolo, M Lerone, et al.
Clinical Genetics|December 1, 1986
Asymmetric crying facies with microcephaly and mental retardation. An autosomal dominant syndrome with variable expressivityM C Silengo, G L Bell, M Biagioli, et al.
Nature Communications|March 17, 2021
Ground deformation reveals the scale-invariant conduit dynamics driving explosive basaltic eruptionsM Ripepe, G Lacanna, M Pistolesi, et al.
Clinical Genetics|February 10, 2016
Fetal growth patterns in Beckwith-Wiedemann syndromeA Mussa, S Russo, A de Crescenzo, et al.
Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.
Pageof 3