Friedrich U - Search Results

1

Linkage analysis between manic-depressive illness and markers on the long arm of chromosome 11.

Ewald H, Mors O, Flint T, Friedrich U, Eiberg H, Kruse TA. Ewald H, et al. Among authors: friedrich u. Am J Med Genet. 1995 Oct 9;60(5):386-92. doi: 10.1002/ajmg.1320600508. Am J Med Genet. 1995. PMID: 8546151

2

Systematic chromosome examination of two families with schizophrenia and two families with manic depressive illness.

Friedrich U, Mors O, Ewald H. Friedrich U, et al. Am J Med Genet. 1996 Feb 16;67(1):58-62. doi: 10.1002/(SICI)1096-8628(19960216)67:1<58::AID-AJMG10>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8678116

3

Exclusion of linkage between manic depressive illness and tyrosine hydroxylase and dopamine D2 receptor genes.

Ewald H, Mors O, Friedrich U, Flint T, Kruse T. Ewald H, et al. Among authors: friedrich u. Psychiatr Genet. 1994 Spring;4(1):13-22. doi: 10.1097/00041444-199421000-00003. Psychiatr Genet. 1994. PMID: 7914141

4

X-linked retinitis pigmentosa: new map studies of XLRP2, and a possible human centromere effect.

Friedrich U, Warburg M, Kruse TA, Andréasson S. Friedrich U, et al. Hum Genet. 1992 Mar;88(6):683-7. doi: 10.1007/BF02265297. Hum Genet. 1992. PMID: 1551673

5

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: friedrich u. 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.

6

Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.

Gravholt CH, Friedrich U. Gravholt CH, et al. Among authors: friedrich u. Am J Med Genet. 1995 Mar 13;56(1):106-11. doi: 10.1002/ajmg.1320560124. Am J Med Genet. 1995. PMID: 7747772 Review.

7

Fluorescence in situ hybridization reveals a break in the alpha-satellite DNA of chromosome 1 in a family with a balanced whole-arm translocation.

Gravholt CH, Caprani M, Friedrich U. Gravholt CH, et al. Among authors: friedrich u. Hum Genet. 1994 Nov;94(5):504-8. doi: 10.1007/BF00211015. Hum Genet. 1994. PMID: 7959684

8

Extreme variant of the short arm of chromosome 15.

Friedrich U, Caprani M, Niebuhr E, Therkelsen AJ, Jørgensen AL. Friedrich U, et al. Hum Genet. 1996 Jun;97(6):710-3. doi: 10.1007/BF02346177. Hum Genet. 1996. PMID: 8641684

9

Occurrence of cancer in a cohort of 183 persons with constitutional chromosome 7 abnormalities.

Hasle H, Olsen JH, Hansen J, Friedrich U, Tommerup N. Hasle H, et al. Among authors: friedrich u. Cancer Genet Cytogenet. 1998 Aug;105(1):39-42. doi: 10.1016/s0165-4608(98)00007-7. Cancer Genet Cytogenet. 1998. PMID: 9689928 Review.

10

Microdissection of chromosome 2--between-arm intrachromosomal insertion.

Friedrich U, Houman M, Sandgaard J, Rosgaard A, Sunde L. Friedrich U, et al. Eur J Hum Genet. 2000 May;8(5):393-5. doi: 10.1038/sj.ejhg.5200421. Eur J Hum Genet. 2000. PMID: 10854102

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