Friedrich U - Search Results

1

Chromosomal studies of children with developmental language retardation.

Friedrich U, Dalby M, Staehelin-Jensen T, Bruun-Petersen G. Friedrich U, et al. Dev Med Child Neurol. 1982 Oct;24(5):645-52. doi: 10.1111/j.1469-8749.1982.tb13675.x. Dev Med Child Neurol. 1982. PMID: 7141121 No abstract available.

2

Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

Bugge M, Bruun-Petersen G, Brøndum-Nielsen K, Friedrich U, Hansen J, Jensen G, Jensen PK, Kristoffersson U, Lundsteen C, Niebuhr E, Rasmussen KR, Rasmussen K, Tommerup N. Bugge M, et al. Among authors: friedrich u. J Med Genet. 2000 Nov;37(11):858-65. doi: 10.1136/jmg.37.11.858. J Med Genet. 2000. PMID: 11073540 Free PMC article.

3

Familial cranial diabetes insipidus: a report of five families. Genetic, diagnostic and therapeutic aspects.

Pedersen EB, Lamm LU, Albertsen K, Madsen M, Bruun-Petersen G, Henningsen K, Friedrich U, Magnusson K. Pedersen EB, et al. Among authors: friedrich u. Q J Med. 1985 Dec;57(224):883-96. Q J Med. 1985. PMID: 4095258

4

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

5

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.

6

Three large Danish families with a paracentric inversion in the short arm of chromosome N. 5.

Baggesen K, Friedrich U, Jensen PK, Rasmussen K. Baggesen K, et al. Among authors: friedrich u. Ann Genet. 1988;31(1):50-2. Ann Genet. 1988. PMID: 3258494

7

Occurrence of cancer in women with Turner syndrome.

Hasle H, Olsen JH, Nielsen J, Hansen J, Friedrich U, Tommerup N. Hasle H, et al. Among authors: friedrich u. Br J Cancer. 1996 May;73(9):1156-9. doi: 10.1038/bjc.1996.222. Br J Cancer. 1996. PMID: 8624281 Free PMC article.

8

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: friedrich u. Eur J Hum Genet. 1996;4(3):160-7. doi: 10.1159/000472190. Eur J Hum Genet. 1996. PMID: 8840116

9

Microdissection - a precise method to disclose the parental origin of supernumerary marker chromosomes.

Friedrich U, Bugge M, Houman M, Friis Henriksen K, Brøndum-Nielsen K. Friedrich U, et al. Ann Genet. 2000 Apr-Jun;43(2):109-10. doi: 10.1016/s0003-3995(00)01015-7. Ann Genet. 2000. PMID: 10998454 No abstract available.

10

Breakpoints around the HOXD cluster result in various limb malformations.

Dlugaszewska B, Silahtaroglu A, Menzel C, Kübart S, Cohen M, Mundlos S, Tümer Z, Kjaer K, Friedrich U, Ropers HH, Tommerup N, Neitzel H, Kalscheuer VM. Dlugaszewska B, et al. Among authors: friedrich u. J Med Genet. 2006 Feb;43(2):111-8. doi: 10.1136/jmg.2005.033555. Epub 2005 Jun 24. J Med Genet. 2006. PMID: 15980115 Free PMC article.

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