Binkert F - Search Results

1

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

2

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.

Robinson WP, Bottani A, Xie YG, Balakrishman J, Binkert F, Mächler M, Prader A, Schinzel A. Robinson WP, et al. Among authors: binkert f. Am J Hum Genet. 1991 Dec;49(6):1219-34. Am J Hum Genet. 1991. PMID: 1684085 Free PMC article.

3

Partial trisomy of chromosome 18 (pter----q12) following a familial 18;21 translocation rcp(18;21)(q12;q11).

Binkert F, Stranzinger J, Schinzel A. Binkert F, et al. Hum Hered. 1990;40(2):81-4. doi: 10.1159/000153910. Hum Hered. 1990. PMID: 2335369

4

An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features.

Schinzel AA, Robinson WP, Binkert F, Fanconi A. Schinzel AA, et al. Among authors: binkert f. Clin Dysmorphol. 1994 Jan;3(1):63-9. Clin Dysmorphol. 1994. PMID: 7515753

5

Intrachromosomal triplication of 15q11-q13.

Schinzel AA, Brecevic L, Bernasconi F, Binkert F, Berthet F, Wuilloud A, Robinson WP. Schinzel AA, et al. Among authors: binkert f. J Med Genet. 1994 Oct;31(10):798-803. doi: 10.1136/jmg.31.10.798. J Med Genet. 1994. PMID: 7837257 Free PMC article.

6

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

Robinson WP, Binkert F, Bernasconi F, Lorda-Sanchez I, Werder EA, Schinzel AA. Robinson WP, et al. Among authors: binkert f. Am J Hum Genet. 1995 Feb;56(2):444-51. Am J Hum Genet. 1995. PMID: 7847381 Free PMC article.

7

Clinical and molecular analysis of five inv dup(15) patients.

Robinson WP, Binkert F, Giné R, Vazquez C, Müller W, Rosenkranz W, Schinzel A. Robinson WP, et al. Among authors: binkert f. Eur J Hum Genet. 1993;1(1):37-50. doi: 10.1159/000472386. Eur J Hum Genet. 1993. PMID: 8069650

8

Parental origin of the supernumerary chromosome in trisomy 18.

Ya-gang X, Robinson WP, Spiegel R, Binkert F, Ruefenacht U, Schinzel AA. Ya-gang X, et al. Among authors: binkert f. Clin Genet. 1993 Aug;44(2):57-61. doi: 10.1111/j.1399-0004.1993.tb03847.x. Clin Genet. 1993. PMID: 8275560

9

Exclusively paternal X chromosomes in a girl with short stature.

Schinzel AA, Robinson WP, Binkert F, Torresani T, Werder EA. Schinzel AA, et al. Among authors: binkert f. Hum Genet. 1993 Sep;92(2):175-8. doi: 10.1007/BF00219687. Hum Genet. 1993. PMID: 8370585

10

Molecular studies of translocations and trisomy involving chromosome 13.

Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA. Robinson WP, et al. Among authors: binkert f. Am J Med Genet. 1996 Jan 11;61(2):158-63. doi: 10.1002/(SICI)1096-8628(19960111)61:2<158::AID-AJMG11>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8669444

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