Author:
Amor David J.,Stephenson Sarah E.M.,Mustapha Mirna,Mensah Martin A.,Ockeloen Charlotte W.,Lee Wei Shern,Tankard Rick M.,Phelan Dean G.,Shinawi Marwan,de Brouwer Arjan P.M.,Pfundt Rolph,Dowling Cari,Toler Tomi L.,Sutton V. Reid,Agolini Emanuele,Rinelli Martina,Capolino Rossella,Martinelli Diego,Zampino Giuseppe,Dumić Miroslav,Reardon William,Shaw-Smith Charles,Leventer Richard J.,Delatycki Martin B.,Kleefstra Tjitske,Mundlos Stefan,Mortier Geert,Bahlo Melanie,Allen Nicola J.,Lockhart Paul J.
Funder
Australian Government National Health and Medical Research Council
National Health and Medical Research Council (NHMRC) Career Development Fellowship
NHMRC senior research fellowship
NHMRC program grant
Independent Research Institute Infrastructure Support Scheme
Victorian State Government Operational Infrastructure Program
BIH Charité Junior Clinician Scientist Program
Charité—Universitätsmediz
Berlin Institute of Health
National Human Genome Research Institute
NHGRI
National Institutes of Health National Institute of Neurological Disorders and Stroke
NIH-NINDS
National Institute on Deafness and other Communicative Disorders
Subject
Genetics (clinical),Genetics
Reference38 articles.
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3. Keipert syndrome in two brothers from Turkey;Balci;Clin. Genet.,1996
4. Additional case of Keipert syndrome and review of the literature;Cappon;Med. Sci. Monit.,2000
5. Broad thumbs and halluces with deafness: a patient with Keipert syndrome;Reardon;Am. J. Med. Genet. A.,2003
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