Friedrich U - Search Results

1

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

2

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

3

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

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

X-inactivation pattern in carriers of X-linked retinitis pigmentosa: a valuable means of prognostic evaluation?

Friedrich U, Warburg M, Jørgensen AL. Friedrich U, et al. Hum Genet. 1993 Oct;92(4):359-63. doi: 10.1007/BF01247335. Hum Genet. 1993. PMID: 8225316

6

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

7

Parental origin of the X chromosome, X chromosome mosaicism and screening for "hidden" Y chromosome in 45,X Turner syndrome ascertained cytogenetically.

Larsen T, Gravholt CH, Tillebeck A, Larsen H, Jensen MB, Nielsen J, Friedrich U. Larsen T, et al. Among authors: friedrich u. Clin Genet. 1995 Jul;48(1):6-11. doi: 10.1111/j.1399-0004.1995.tb04046.x. Clin Genet. 1995. PMID: 7586647

8

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.

9

Diagnostic reliability of the cytogenetic centromere heteromorphism in the human X chromosome.

Friedrich U, Larsen TB, Nielsen J. Friedrich U, et al. Clin Genet. 1991 Dec;40(6):465-6. doi: 10.1111/j.1399-0004.1991.tb03119.x. Clin Genet. 1991. PMID: 1685701

10

Unusual segregation in a family with a 11/21 translocation.

Steensen P, Ford JH, Lillquist K, Friedrich U. Steensen P, et al. Among authors: friedrich u. Clin Genet. 1988 Jun;33(6):449-53. doi: 10.1111/j.1399-0004.1988.tb03479.x. Clin Genet. 1988. PMID: 3168317

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