Binkert F - Search Results

1

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

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

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.

5

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.

6

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

7

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

8

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.

9

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

10

A 5-year-old girl with interstitial deletion of 3p14: clinical, psychologic, cytogenetic, and molecular studies.

Schinzel A, Gundelfinger R, Dutly F, Baumer A, Binkert F. Schinzel A, et al. Among authors: binkert f. Am J Med Genet. 1998 May 26;77(4):302-5. Am J Med Genet. 1998. PMID: 9600740

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