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524 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: hennekam rc. Am J Med Genet. 1998 Mar 19;76(3):262-8. Am J Med Genet. 1998. PMID: 9508247 Review.
Aplasia cutis congenita reminiscent of the lines of Blaschko.
Hennekam RC. Hennekam RC. Hum Genet. 1992 Dec;90(4):469-71. doi: 10.1007/BF00220481. Hum Genet. 1992. PMID: 1483708
Congenital glaucoma in a child with partial 1q duplication and 9p deletion.
Verbraak FD, Pogány K, Pilon JW, Mooy CM, de France HF, Hennekam RC, Bleeker-Wagemakers EM. Verbraak FD, et al. Among authors: hennekam rc. Ophthalmic Paediatr Genet. 1992 Sep;13(3):165-70. doi: 10.3109/13816819209046485. Ophthalmic Paediatr Genet. 1992. PMID: 1484694
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: hennekam rc. 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.
Dominantly inherited microcephaly, short stature and normal intelligence.
Hennekam RC, van Rhijn A, Hennekam FA. Hennekam RC, et al. Among authors: hennekam fa. Clin Genet. 1992 May;41(5):248-51. doi: 10.1111/j.1399-0004.1992.tb03675.x. Clin Genet. 1992. PMID: 1606714
Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
van Balkom ID, Hagendoorn J, De Pater JM, Hennekam RC. van Balkom ID, et al. Among authors: hennekam rc. Genet Couns. 1992;3(2):83-9. Genet Couns. 1992. PMID: 1642815 Review.
A case with laryngeal atresia and partial trisomy 9 due to maternal 9;16 translocation.
Van den Boogaard MJ, De Pater J, Hennekam RC. Van den Boogaard MJ, et al. Among authors: hennekam rc. Genet Couns. 1991;2(2):83-91. Genet Couns. 1991. PMID: 1781959
Familial holoprosencephaly, heart defects, and polydactyly.
Hennekam RC, van Noort G, de la Fuente AA. Hennekam RC, et al. Am J Med Genet. 1991 Nov 1;41(2):258-62. doi: 10.1002/ajmg.1320410226. Am J Med Genet. 1991. PMID: 1785646 Review.
Hereditary multiple exostoses.
Hennekam RC. Hennekam RC. J Med Genet. 1991 Apr;28(4):262-6. doi: 10.1136/jmg.28.4.262. J Med Genet. 1991. PMID: 1856833 Free PMC article. No abstract available.
Short rib syndrome--Beemer type in sibs.
Hennekam RC. Hennekam RC. Am J Med Genet. 1991 Aug 1;40(2):230-3. doi: 10.1002/ajmg.1320400221. Am J Med Genet. 1991. PMID: 1897578 Review.
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