De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature
Velagaleti, GVN, Jalal, SM, Kukolich, MK, Lockhart, LH, Tonk, VS
Published in Clinical genetics (01.03.2002)
Published in Clinical genetics (01.03.2002)
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Ring chromosome 8 syndrome: further characterization
Tonk, V S, Kukolich, M K, Morgan, D, Khan, A, Jalal, S M
Published in American journal of medical genetics (17.01.2000)
Published in American journal of medical genetics (17.01.2000)
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Tetrasomy 9p: an emerging syndrome
Jalal, S M, Kukolich, M K, Garcia, M, Benjamin, T R, Day, D W
Published in Clinical genetics (01.01.1991)
Published in Clinical genetics (01.01.1991)
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Mosaic Down's syndrome with de novo 45,XX,-21,-22,+t(21q;22q)/46,XX,-21,+t(21q;21q) rearrangement
Tharapel, A T, Redheendran, R, Mankinen, C B, Kukolich, M K
Published in Journal of medical genetics (01.10.1984)
Published in Journal of medical genetics (01.10.1984)
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Retinal pigment mosaicism in Pallister-Killian syndrome (mosaic tetrasomy 12p)
Graham, W, Brown, S M, Shah, F, Tonk, V S, Kukolich, M K
Published in Archives of ophthalmology (1960) (01.12.1999)
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Published in Archives of ophthalmology (1960) (01.12.1999)
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De novo partial duplications 1p: report of two new cases and review
Garcia-Heras, J, Corley, N, Garcia, M F, Kukolich, M K, Smith, K G, Day, D W
Published in American journal of medical genetics (29.01.1999)
Published in American journal of medical genetics (29.01.1999)
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Euchromatic 9q + heteromorphism in a family
Jalal, S M, Kukolich, M K, Garcia, M, Day, D W
Published in American journal of medical genetics (01.09.1990)
Published in American journal of medical genetics (01.09.1990)
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Trisomy 22: no longer an enigma
Kukolich, M K, Kulharya, A, Jalal, S M, Drummond-Borg, M
Published in American journal of medical genetics (01.12.1989)
Published in American journal of medical genetics (01.12.1989)
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Hypomelanosis of Ito with triphalangeal thumbs
Kukolich, M K, Althaus, B W, Freeman, M V, Lewandowski, R C
Published in Journal of medical genetics (01.04.1980)
Published in Journal of medical genetics (01.04.1980)
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Euchromatic 16p+ heteromorphism: first report in North America
Jalal, S M, Schneider, N R, Kukolich, M K, Wilson, G N
Published in American journal of medical genetics (01.12.1990)
Published in American journal of medical genetics (01.12.1990)
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Abnormalities resulting from a familial pericentric inversion of chromosome 18
Kukolich, M K, Althaus, B W, Sears, J W, Mankinen, C B, Lewandowski, R C
Published in Clinical genetics (01.08.1978)
Published in Clinical genetics (01.08.1978)
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Prenatal diagnosis of a de novo trisomy 6q22.2-->6qter and monosomy 1pter-->1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q
Kulharya, A S, Carlin, M E, Stettler, R W, Huslig, M, Kukolich, M K, Garcia-Heras, J, Stettler, W A
Published in Clinical genetics (01.02.1997)
Published in Clinical genetics (01.02.1997)
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Tetraploidy: a report of three live-born infants
Scarbrough, P R, Hersh, J, Kukolich, M K, Carroll, A J, Finley, S C, Hochberger, R, Wilkerson, S, Yen, F F, Althaus, B W
Published in American journal of medical genetics (01.09.1984)
Published in American journal of medical genetics (01.09.1984)
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Partial deletion 10q
Lewandowski, Jr, R C, Kukolich, M K, Sears, J W, Mankinen, C B
Published in Human genetics (01.01.1978)
Published in Human genetics (01.01.1978)
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