Hochstenbach PF - Search Results

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[Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping].

Franssen MT, Korevaar JC, Leschot NJ, Bossuyt PM, Knegt AC, Gerssen-Schoorl KB, Wouters CH, Hansson KB, Hochstenbach PF, Madan K, van der Veen F, Goddijn M. Franssen MT, et al. Among authors: hochstenbach pf. Ned Tijdschr Geneeskd. 2007 Apr 14;151(15):863-7. Ned Tijdschr Geneeskd. 2007. PMID: 17472118 Dutch.

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.

Vorstman JA, Staal WG, van Daalen E, van Engeland H, Hochstenbach PF, Franke L. Vorstman JA, et al. Among authors: hochstenbach pf. Mol Psychiatry. 2006 Jan;11(1):1, 18-28. doi: 10.1038/sj.mp.4001781. Mol Psychiatry. 2006. PMID: 16205736 Review.

Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome.

Flipsen-ten Berg K, van Hasselt PM, Eleveld MJ, van der Wijst SE, Hol FA, de Vroede MA, Beemer FA, Hochstenbach PF, Poot M. Flipsen-ten Berg K, et al. Among authors: hochstenbach pf. Eur J Hum Genet. 2007 Nov;15(11):1132-8. doi: 10.1038/sj.ejhg.5201899. Epub 2007 Jul 18. Eur J Hum Genet. 2007. PMID: 17637805

Demonstration of X chromatin in drumstick-like nuclear appendages of leukocytes by in situ hybridization on blood smears.

Hochstenbach PF, Scheres JM, Hustinx TW, Wieringa B. Hochstenbach PF, et al. Histochemistry. 1986;84(4-6):383-6. doi: 10.1007/BF00482967. Histochemistry. 1986. PMID: 3721910

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