Binkert F - Search Results

1

Contamination of amniotic fluid with maternal balanced t(11;22) translocation cells.

Fokstuen S, Binkert F, Munoz A, Erb N, Dürig P, Altermatt HJ, Blouin JL, Kotzot D. Fokstuen S, et al. Among authors: binkert f. Am J Med Genet A. 2013 May;161A(5):1101-4. doi: 10.1002/ajmg.a.35774. Epub 2013 Feb 26. Am J Med Genet A. 2013. PMID: 23444046 No abstract available.

2

Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically.

Blouin JL, Binkert F, Antonarakis SE. Blouin JL, et al. Among authors: binkert f. Am J Med Genet. 1994 Feb 1;49(3):363-8. doi: 10.1002/ajmg.1320490333. Am J Med Genet. 1994. PMID: 8209906

3

Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.

Schinzel A, Kotzot D, Brecevic L, Robinson WP, Dutly F, Dauwerse H, Binkert F, Baumer A, Ausserer B. Schinzel A, et al. Among authors: binkert f. Eur J Hum Genet. 1997 Sep-Oct;5(5):308-14. Eur J Hum Genet. 1997. PMID: 9412788

4

Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation.

Zimmermann-Bär U, Stallmach T, Riegel M, Wiedemann U, Fauchère JC, Binkert F, Kotzot D. Zimmermann-Bär U, et al. Among authors: binkert f. Prenat Diagn. 2000 Oct;20(10):847-50. doi: 10.1002/1097-0223(200010)20:10<847::aid-pd930>3.0.co;2-o. Prenat Diagn. 2000. PMID: 11038468

5

No evidence of dup(7)(p11.2p13) in Silver-Russell syndrome.

Martinez MJ, Binkert F, Schinzel A, Kotzot D. Martinez MJ, et al. Among authors: binkert f. Am J Med Genet. 2001 Apr 1;99(4):335-7. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1177>3.0.co;2-q. Am J Med Genet. 2001. PMID: 11252004 No abstract available.

6

Parental origin and mechanism of formation of a 46,X,der(X)(pter-->q21.1::p11.4-->pter)/45,X karyotype in a woman with mild Turner syndrome.

Binkert F, Spreiz A, Höckner M, Miny P, von Dach Leu B, Erdel M, Zschocke J, Utermann G, Kotzot D. Binkert F, et al. Fertil Steril. 2010 Jun;94(1):350.e12-5. doi: 10.1016/j.fertnstert.2009.12.040. Epub 2010 Feb 1. Fertil Steril. 2010. PMID: 20117774 Free article.

7

Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.

Röthlisberger B, Kotzot D, Brecevic L, Koehler M, Balmer D, Binkert F, Schinzel A. Röthlisberger B, et al. Among authors: binkert f. Eur J Hum Genet. 1999 Dec;7(8):873-83. doi: 10.1038/sj.ejhg.5200389. Eur J Hum Genet. 1999. PMID: 10602362

8

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications.

Kotzot D, Martinez MJ, Bagci G, Basaran S, Baumer A, Binkert F, Brecevic L, Castellan C, Chrzanowska K, Dutly F, Gutkowska A, Karaüzüm SB, Krajewska-Walasek M, Luleci G, Miny P, Riegel M, Schuffenhauer S, Seidel H, Schinzel A. Kotzot D, et al. Among authors: binkert f. J Med Genet. 2000 Apr;37(4):281-6. doi: 10.1136/jmg.37.4.281. J Med Genet. 2000. PMID: 10745046 Free PMC article.

9

Kallmann syndrome in a boy with a t(1;10) translocation detected by reverse chromosome painting.

Schinzel A, Lorda-Sanchez I, Binkert F, Carter NP, Bebb CE, Ferguson-Smith MA, Eiholzer U, Zachmann M, Robinson WP. Schinzel A, et al. Among authors: binkert f. J Med Genet. 1995 Dec;32(12):957-61. doi: 10.1136/jmg.32.12.957. J Med Genet. 1995. PMID: 8825924 Free PMC article.

10

Interstitial deletion, del(4)(q12q21.1), owing to de novo unbalanced translocation in a 2 year old girl: further evidence that the piebald trait maps to proximal 4q12.

Schinzel A, Braegger CP, Brecevic L, Dutly F, Binkert F. Schinzel A, et al. Among authors: binkert f. J Med Genet. 1997 Aug;34(8):692-5. doi: 10.1136/jmg.34.8.692. J Med Genet. 1997. PMID: 9279767 Free PMC article.

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