Beensen V - Search Results

1

Evidence for a new microdeletion syndrome in 15q21.

Liehr T, Starke H, Heller A, Weise A, Beensen V, Senger G, Kittner G, Prechtel M, Claussen U, Seidel J. Liehr T, et al. Among authors: beensen v. Int J Mol Med. 2003 May;11(5):575-7. doi: 10.3892/ijmm.11.5.575. Int J Mol Med. 2003. PMID: 12684692

2

Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.

Liehr T, Starke H, Beensen V, Kähler C, Harbich M, Brude E, Ziegler M, Claussen U. Liehr T, et al. Among authors: beensen v. Int J Mol Med. 1999 Jan;3(1):11-4. doi: 10.3892/ijmm.3.1.11. Int J Mol Med. 1999. PMID: 9864379

3

First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16.

Starke H, Mitulla B, Nietzel A, Heller A, Beensen V, Grosswendt G, Claussen U, von Eggeling F, Liehr T. Starke H, et al. Among authors: beensen v. Am J Med Genet A. 2003 Jan 1;116A(1):26-30. doi: 10.1002/ajmg.a.10830. Am J Med Genet A. 2003. PMID: 12476447

4

A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Seidel J, Heller A, Senger G, Starke H, Chudoba I, Kelbova C, Tönnies H, Neitzel H, Haase C, Beensen V, Zintl F, Claussen U, Liehr T. Seidel J, et al. Among authors: beensen v. Eur J Pediatr. 2003 Sep;162(9):582-8. doi: 10.1007/s00431-003-1254-3. Epub 2003 Jun 19. Eur J Pediatr. 2003. PMID: 12819962 Review.

5

Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotype.

Schreyer I, Neumann A, Beensen V, Eichhorn KH, Heller A, Claussen U, Liehr T. Schreyer I, et al. Among authors: beensen v. J Histochem Cytochem. 2005 Mar;53(3):365-6. doi: 10.1369/jhc.4B6388.2005. J Histochem Cytochem. 2005. PMID: 15750021

6

Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.

Rubtsov N, Senger G, Kuzcera H, Neumann A, Kelbova C, Junker K, Beensen V, Claussen U. Rubtsov N, et al. Among authors: beensen v. Hum Genet. 1996 Jun;97(6):705-9. doi: 10.1007/BF02346176. Hum Genet. 1996. PMID: 8641683

7

Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life.

Hübler A, Seidel J, Kauf E, Schramm D, Beensen V, Heller A, Liehr T, Zintl F. Hübler A, et al. Among authors: beensen v. J Pediatr Endocrinol Metab. 2000 Apr;13(4):445-50. doi: 10.1515/jpem.2000.13.4.445. J Pediatr Endocrinol Metab. 2000. PMID: 10777002

8

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.

Heller A, Seidel J, Hübler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. Heller A, et al. Among authors: beensen v. J Med Genet. 2000 Jul;37(7):529-32. doi: 10.1136/jmg.37.7.529. J Med Genet. 2000. PMID: 10882757 Free PMC article.

9

Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome.

Dufke A, Seidel J, Schöning M, Döbler-Neumann M, Kelbova C, Liehr T, Beensen V, Backsch C, Klein-Vogler U, Enders H. Dufke A, et al. Among authors: beensen v. Cytogenet Cell Genet. 2000;91(1-4):81-4. doi: 10.1159/000056823. Cytogenet Cell Genet. 2000. PMID: 11173835

10

Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.

Starke H, Schreyer I, Kähler C, Fiedler W, Beensen V, Heller A, Nietzel A, Claussen U, Liehr T. Starke H, et al. Among authors: beensen v. Prenat Diagn. 1999 Dec;19(12):1169-74. Prenat Diagn. 1999. PMID: 10590438 Review.

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