Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation
Pettenati, M J, Rao, N, Johnson, C, Hayworth, R, Crandall, K, Huff, O, Thomas, I T
Published in Human genetics (01.08.1992)
Published in Human genetics (01.08.1992)
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Journal Article
Williams syndrome: autosomal dominant inheritance
Morris, C A, Thomas, I T, Greenberg, F
Published in American journal of medical genetics (15.09.1993)
Published in American journal of medical genetics (15.09.1993)
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Journal Article
New lethal syndrome of fetal akinesia with characteristic facial appearance, severe microphthalmia, microtia, and truncus arteriosus in two male sibs
Thomas, I T, Jewett, T, Raines, K H, Gash, C, Garber, P
Published in American journal of medical genetics (15.04.1993)
Published in American journal of medical genetics (15.04.1993)
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Journal Article
De novo inv(2)(p21q31) associated with isolated bilateral microphthalmia and cataracts
Weaver, R G, Rao, N, Thomas, I T, Pettenati, M J
Published in American journal of medical genetics (15.09.1991)
Published in American journal of medical genetics (15.09.1991)
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Journal Article
Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23
Jewett, T, Rao, P N, Weaver, R G, Stewart, W, Thomas, I T, Pettenati, M J
Published in American journal of medical genetics (01.12.1993)
Published in American journal of medical genetics (01.12.1993)
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Journal Article
Libro de proprietatibus rerum en romance
en casa de Gaspar de Auila...: a costa y espensas del noble varon Ioan Thomas Fabio, Gaspar de Ávila (Toledo), Giovanni Tomaso Fabio (Toledo), Antonio Hernández Morejón BHI BH MED 22, Francisco Guerra BHI BH FG 1304
Year of defence 1529
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Year of defence 1529
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