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Results of search for 'au:"Stanghellini, I"'
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Authors
Ambrosetti, F
Bertorelli, R
Capone, L
Falcinelli, C
Forabosco, A
Garavelli, L
Genovese, E
Mazza, V
Neri, C
Palma, S
Percesepe, A
Presutti, L
Stanghellini, I
Varriale, L
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Topics
3' Flanking Region
Abortion, Eugenic
Aged
Child
Chromosomes, Human, Y
Connexin 26
Connexins
Consanguinity
DNA
DNA Probes
Deleted in Azoospermia 1 Protein
Dwarfism
Enhancer Elements, Genetic
Female
Gene Deletion
Humans
Male
Pedigree
Pregnancy
genetics
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English
Your search returned 3 results.
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1.
A mild phenotype of sensorineural hearing loss and palmoplantar keratoderma caused by a novel GJB2 dominant mutation.
[electronic resource]
by
Stanghellini, I
Genovese, E
Palma, S
Falcinelli, C
Presutti, L
Percesepe, A
Producer:
20180628
In:
Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale
vol. 37
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2.
Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe.
[electronic resource]
by
Stanghellini, I
Bertorelli, R
Capone, L
Mazza, V
Neri, C
Percesepe, A
Forabosco, A
Producer:
20061114
In:
Molecular human reproduction
vol. 12
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3.
The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia.
[electronic resource]
by
Bertorelli, R
Capone, L
Ambrosetti, F
Garavelli, L
Varriale, L
Mazza, V
Stanghellini, I
Percesepe, A
Forabosco, A
Producer:
20080104
In:
Clinical genetics
vol. 72
Online resources:
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