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J G A M Heister

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TOP 3
Barbara Franke; M Hoogman; A Arias Vasquez; J G A M Heister; P J Savelkoul; M Naber; Hans Scheffer; L A Kiemeney; Cornelis C Kan; J J S Kooij; Jan K Buitelaar
Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.
Ersan Kalay; Refik Caylan; A F Kiroglu; tekin yasar; Rob W J Collin; J G A M Heister; Jaap Oostrik; Cor W R J Cremers; Han G Brunner; Ahmet Karaguzel; Hannie Kremer
A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.
Ersan Kalay; Arjan de Brouwer; Refik Caylan; Sander B Nabuurs; Bernd Wollnik; Ahmet Karaguzel; J G A M Heister; Hidayet Erdol; Frans P M Cremers; Cor W R J Cremers; Han G Brunner; Hannie Kremer
A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome.

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All Publications

2008: Barbara Franke; M Hoogman; A Arias Vasquez; J G A M Heister; P J Savelkoul; M Naber; Hans Scheffer; L A Kiemeney; Cornelis C Kan; J J S Kooij; Jan K Buitelaar
Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(8):1576-9.
2007: Ersan Kalay; Refik Caylan; A F Kiroglu; tekin yasar; Rob W J Collin; J G A M Heister; Jaap Oostrik; Cor W R J Cremers; Han G Brunner; Ahmet Karaguzel; Hannie Kremer
A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.
Journal of molecular medicine (Berlin, Germany) 2007;85(4):397-404.
2005: Ersan Kalay; Arjan de Brouwer; Refik Caylan; Sander B Nabuurs; Bernd Wollnik; Ahmet Karaguzel; J G A M Heister; Hidayet Erdol; Frans P M Cremers; Cor W R J Cremers; Han G Brunner; Hannie Kremer
A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome.
Journal of molecular medicine (Berlin, Germany) 2005;83(12):1025-32.
2004: Anneke I den Hollander; Janneke J C van Lith-Verhoeven; Ferry F J Kersten; J G A M Heister; Carolien G F de Kovel; August F Deutman; Carel B Hoyng; Frans P M Cremers
Identification of novel locus for autosomal dominant butterfly shaped macular dystrophy on 5q21.2-q33.2.
Journal of medical genetics 2004;41(9):699-702.
2004: Carolien G F de Kovel; Frans A Hol; J G A M Heister; J J H T Willemen; Lodewijk A Sandkuijl; Barbara Franke; George W Padberg
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
Journal of medical genetics 2004;41(9):652-7.

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