Lyngbye T - Search Results

1

Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridia.

Grønskov K, Olsen JH, Sand A, Pedersen W, Carlsen N, Bak Jylling AM, Lyngbye T, Brøndum-Nielsen K, Rosenberg T. Grønskov K, et al. Among authors: lyngbye t. Hum Genet. 2001 Jul;109(1):11-8. doi: 10.1007/s004390100529. Hum Genet. 2001. PMID: 11479730

2

Tetrasomy 18p de novo: parental origin and different mechanisms of formation.

Bugge M, Blennow E, Friedrich U, Petersen MB, Pedeutour F, Tsezou A, Orum A, Hermann S, Lyngbye T, Sarri C, Avramopoulos D, Kitsiou S, Lambert JC, Guzda M, Tommerup N, Brøndum-Nielsen K. Bugge M, et al. Among authors: lyngbye t. Eur J Hum Genet. 1996;4(3):160-7. doi: 10.1159/000472190. Eur J Hum Genet. 1996. PMID: 8840116

3

Value of chromosome painting in determining the chromosomal outcome in offspring of a 12;16 translocation carrier.

Brandt CA, Lyngbye T, Pedersen S, Bolund L, Friedrich U. Brandt CA, et al. Among authors: lyngbye t. J Med Genet. 1994 Mar;31(3):234-7. doi: 10.1136/jmg.31.3.234. J Med Genet. 1994. PMID: 8014973 Free PMC article.

4

Small metacentric nonsatellited extra chromosome: report of five mentally retarded individuals and review of literature. Contribution to further delineation of a new syndrome.

Nielsen KB, Dyggve H, Friedrich U, Hobolth N, Lyngbye T, Mikkelsen M. Nielsen KB, et al. Among authors: lyngbye t. Hum Genet. 1978 Oct 19;44(1):59-69. doi: 10.1007/BF00283575. Hum Genet. 1978. PMID: 711239

5

[Triploidy].

Lyngbye T, Friedrich U. Lyngbye T, et al. Ugeskr Laeger. 1977 Apr 18;139(17):951. Ugeskr Laeger. 1977. PMID: 557854 Danish. No abstract available.

6

The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys.

Ernst A, Le VQ, Højland AT, Pedersen IS, Sørensen TH, Bjerregaard LL, Lyngbye TJ, Gammelager NM, Krarup H, Petersen MB. Ernst A, et al. Among authors: lyngbye tj. Mol Syndromol. 2015 Oct;6(4):181-6. doi: 10.1159/000441047. Epub 2015 Sep 29. Mol Syndromol. 2015. PMID: 26648834 Free PMC article.

7

[Deletion of the short arm of chromosome 7].

Oster J, Lyngbye T, Friedrich U. Oster J, et al. Among authors: lyngbye t. Ugeskr Laeger. 1974 Dec 30;137(1):37. Ugeskr Laeger. 1974. PMID: 4454099 Danish. No abstract available.

8

A girl with karyotype 46,XX,del(7)(qter-p 15:).

Friedrich U, Lyngbye T, Oster J. Friedrich U, et al. Among authors: lyngbye t. Humangenetik. 1975;26(2):161-5. doi: 10.1007/BF00278448. Humangenetik. 1975. PMID: 1112608

9

Use of banding techniques for zygosity diagnosis in twins.

Friedrich U, Lyngbye T, Oster J. Friedrich U, et al. Among authors: lyngbye t. Acta Genet Med Gemellol (Roma). 1977;26(1):89-91. doi: 10.1017/s0001566000010254. Acta Genet Med Gemellol (Roma). 1977. PMID: 71840

10

[Beckwith-Wiedemann syndrome].

Lyngbye T, Friedrich U, Thordal C. Lyngbye T, et al. Ugeskr Laeger. 1985 Aug 19;147(34):2658-61. Ugeskr Laeger. 1985. PMID: 4071701 Danish. No abstract available.

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