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198 results
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Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated cases.
Laan LA, Halley DJ, den Boer AT, Hennekam RC, Renier WO, Brouwer OF. Laan LA, et al. Among authors: brouwer of. Am J Med Genet. 1998 Mar 19;76(3):262-8. Am J Med Genet. 1998. PMID: 9508247 Review.
Oculoauriculovertebral spectrum and cerebral anomalies.
Schrander-Stumpel CT, de Die-Smulders CE, Hennekam RC, Fryns JP, Bouckaert PX, Brouwer OF, da Costa JJ, Lommen EJ, Maaswinkel-Mooy PD. Schrander-Stumpel CT, et al. Among authors: brouwer of. J Med Genet. 1992 May;29(5):326-31. doi: 10.1136/jmg.29.5.326. J Med Genet. 1992. PMID: 1583660 Free PMC article. Review.
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.
Wijmenga C, Sandkuijl LA, Moerer P, van der Boorn N, Bodrug SE, Ray PN, Brouwer OF, Murray JC, van Ommen GJ, Padberg GW, et al. Wijmenga C, et al. Among authors: brouwer of. Am J Hum Genet. 1992 Aug;51(2):411-5. Am J Hum Genet. 1992. PMID: 1642239 Free PMC article.
Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.
Wijmenga C, Frants RR, Brouwer OF, Moerer P, Weber JL, Padberg GW. Wijmenga C, et al. Among authors: brouwer of. Lancet. 1990 Sep 15;336(8716):651-3. doi: 10.1016/0140-6736(90)92148-b. Lancet. 1990. PMID: 1975852
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.
Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA, et al. Wijmenga C, et al. Among authors: brouwer of. Genomics. 1991 Apr;9(4):570-5. doi: 10.1016/0888-7543(91)90348-i. Genomics. 1991. PMID: 2037288
Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5.
Wijmenga C, Frants RR, Brouwer OF, van der Klift HM, Meera Khan P, Padberg GW. Wijmenga C, et al. Among authors: brouwer of. J Neurol Sci. 1990 Feb;95(2):225-9. doi: 10.1016/0022-510x(90)90245-i. J Neurol Sci. 1990. PMID: 2157824
Optic glioma with intraocular tumor and seeding in a child with neurofibromatosis.
de Keizer RJ, de Wolff-Rouendaal D, Bots GT, Thomeer RT, Brouwer OF, Vielvoye GJ. de Keizer RJ, et al. Among authors: brouwer of. Am J Ophthalmol. 1989 Dec 15;108(6):717-25. doi: 10.1016/0002-9394(89)90868-4. Am J Ophthalmol. 1989. PMID: 2512811
Holoprosencephaly: variation of expression in face and brain in three sibs.
Zwetsloot CP, Brouwer OF, Maaswinkel-Mooy PD. Zwetsloot CP, et al. Among authors: brouwer of. J Med Genet. 1989 Apr;26(4):274-6. doi: 10.1136/jmg.26.4.274. J Med Genet. 1989. PMID: 2751762 Free PMC article.
Acute confusional migraine. Case report and review of literature.
Haan J, Ferrari MD, Brouwer OF. Haan J, et al. Among authors: brouwer of. Clin Neurol Neurosurg. 1988;90(3):275-8. doi: 10.1016/0303-8467(88)90037-6. Clin Neurol Neurosurg. 1988. PMID: 3197358
Recurrence risk in the Angelman ("happy puppet") syndrome.
Willems PJ, Dijkstra I, Brouwer OF, Smit GP. Willems PJ, et al. Among authors: brouwer of. Am J Med Genet. 1987 Aug;27(4):773-80. doi: 10.1002/ajmg.1320270405. Am J Med Genet. 1987. PMID: 3321989 Review.
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