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F Lalatta

Showing results (11-20 of 42) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Odontochondrodysplasia]P Maroteaux, V Briscioli, F Lalatta, et al.
Mondo Ortodontico|March 1, 1987
[Identification in utero of malformations of the 1st brachial arch]G P Farronato, R Giudici, F Lalatta, et al.
Prenatal Diagnosis|September 22, 1998
Prenatal diagnosis of genetic syndromes may be facilitated by serendipitous findings at fetal blood samplingF Lalatta, S Salmona, R Fogliani, et al.
Fertility and Sterility|October 1, 1992
Fertility in a 47,XXY patient: assessment of biological paternity by deoxyribonucleic acid fingerprintingG Terzoli, F Lalatta, A Lobbiani, et al.
American Journal of Medical Genetics|July 31, 1995
Kaufman oculocerebrofacial syndrome in a girl of 15 yearsV Briscioli, S Manoukian, A Selicorni, et al.
Journal of Medical Genetics|July 1, 1993
Trisomy 10qter confirmed by in situ hybridisationV Briscioli, G Floridia, E Rossi, et al.
Prenatal Diagnosis|February 1, 1992
First-trimester prenatal diagnosis of Roberts syndromeS Stioui, O Privitera, B Brambati, et al.
American Journal of Medical Genetics|May 17, 1996
Cardio-facio-cutaneous (CFC) syndrome: report of an adult without mental retardationS Manoukian, F Lalatta, A Selicorni, et al.
Clinical Genetics|November 27, 1998
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutationS Russo, V Briscioli, F Cogliati, et al.
Clinical Genetics|February 1, 1981
Alpha 1-antitrypsin in patients with hepatocellular carcinoma and chronic active hepatitisS Fargion, E C Klasen, F Lalatta, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Odontochondrodysplasia]P Maroteaux, V Briscioli, F Lalatta, et al.
Mondo Ortodontico|March 1, 1987
[Identification in utero of malformations of the 1st brachial arch]G P Farronato, R Giudici, F Lalatta, et al.
Prenatal Diagnosis|September 22, 1998
Prenatal diagnosis of genetic syndromes may be facilitated by serendipitous findings at fetal blood samplingF Lalatta, S Salmona, R Fogliani, et al.
Fertility and Sterility|October 1, 1992
Fertility in a 47,XXY patient: assessment of biological paternity by deoxyribonucleic acid fingerprintingG Terzoli, F Lalatta, A Lobbiani, et al.
American Journal of Medical Genetics|July 31, 1995
Kaufman oculocerebrofacial syndrome in a girl of 15 yearsV Briscioli, S Manoukian, A Selicorni, et al.
Journal of Medical Genetics|July 1, 1993
Trisomy 10qter confirmed by in situ hybridisationV Briscioli, G Floridia, E Rossi, et al.
Prenatal Diagnosis|February 1, 1992
First-trimester prenatal diagnosis of Roberts syndromeS Stioui, O Privitera, B Brambati, et al.
American Journal of Medical Genetics|May 17, 1996
Cardio-facio-cutaneous (CFC) syndrome: report of an adult without mental retardationS Manoukian, F Lalatta, A Selicorni, et al.
Clinical Genetics|November 27, 1998
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutationS Russo, V Briscioli, F Cogliati, et al.
Clinical Genetics|February 1, 1981
Alpha 1-antitrypsin in patients with hepatocellular carcinoma and chronic active hepatitisS Fargion, E C Klasen, F Lalatta, et al.
Pageof 5