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A Mesoraca

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Prenatal Diagnosis|December 24, 2003
First report of prenatal diagnosis of genetic congenital deafness in a routine prenatal genetic testM L Santoro, L Mobili, A Mesoraca, et al.
International Journal of Clinical & Laboratory Research|January 1, 1995
Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassayF Sangiuolo, P Maceratesi, A Mesoraca, et al.
Human Mutation|April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. OnlineF Sangiuolo, A Botta, A Mesoraca, et al.
Prenatal Diagnosis|August 1, 1996
Ultrasound and molecular mid-trimester prenatal diagnosis of de novo achondroplasiaA Mesoraca, G Pilu, A Perolo, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Prenatal Diagnosis|December 24, 2003
First report of prenatal diagnosis of genetic congenital deafness in a routine prenatal genetic testM L Santoro, L Mobili, A Mesoraca, et al.
International Journal of Clinical & Laboratory Research|January 1, 1995
Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassayF Sangiuolo, P Maceratesi, A Mesoraca, et al.
Human Mutation|April 24, 1999
Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. OnlineF Sangiuolo, A Botta, A Mesoraca, et al.
Prenatal Diagnosis|August 1, 1996
Ultrasound and molecular mid-trimester prenatal diagnosis of de novo achondroplasiaA Mesoraca, G Pilu, A Perolo, et al.
Pageof 1