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3-M syndrome: description of six new patients with review of the literature.
van der Wal G, Otten BJ, Brunner HG, van der Burgt I. van der Wal G, et al. Among authors: brunner hg. Clin Dysmorphol. 2001 Oct;10(4):241-52. doi: 10.1097/00019605-200110000-00002. Clin Dysmorphol. 2001. PMID: 11665997 Review.
Craniofrontonasal dysplasia.
Kapusta L, Brunner HG, Hamel BC. Kapusta L, et al. Among authors: brunner hg. Eur J Pediatr. 1992 Nov;151(11):837-41. doi: 10.1007/BF01957936. Eur J Pediatr. 1992. PMID: 1468459
Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis.
Semmekrot BA, Haraldsson A, Weemaes CM, Smeets DF, Geven WB, Brunner HG. Semmekrot BA, et al. Among authors: brunner hg. Am J Med Genet. 1992 Mar 1;42(5):736-40. doi: 10.1002/ajmg.1320420523. Am J Med Genet. 1992. PMID: 1632450
Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.
Brunner HG, Winter RM. Brunner HG, et al. J Med Genet. 1991 Jun;28(6):389-94. doi: 10.1136/jmg.28.6.389. J Med Genet. 1991. PMID: 1870095 Free PMC article.
Acrocallosal syndrome.
Hendriks HJ, Brunner HG, Haagen TA, Hamel BC. Hendriks HJ, et al. Among authors: brunner hg. Am J Med Genet. 1990 Mar;35(3):443-6. doi: 10.1002/ajmg.1320350325. Am J Med Genet. 1990. PMID: 2309796
[The De Barsy syndrome].
Hoekx J, Smeitink J, Brunner H, Monnens L. Hoekx J, et al. Tijdschr Kindergeneeskd. 1989 Apr;57(2):53-7. Tijdschr Kindergeneeskd. 1989. PMID: 2741159 Dutch.
Further delineation of the branchio-oculo-facial syndrome.
Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P, et al. Lin AE, et al. Among authors: brunner hg. Am J Med Genet. 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. Am J Med Genet. 1995. PMID: 7747785 Review.
Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier report.
Hamel BC, Draaisma JM, Pinckers AJ, Boetes C, Hoppe RL, Ropers HH, Brunner HG. Hamel BC, et al. Among authors: brunner hg. Am J Med Genet. 1995 Apr 10;56(3):312-6. doi: 10.1002/ajmg.1320560320. Am J Med Genet. 1995. PMID: 7778598 Review.
Aberrant splicing of the COL4A5 gene in patients with Alport syndrome.
Lemmink HH, Kluijtmans LA, Brunner HG, Schröder CH, Knebelmann B, Jelínková E, van Oost BA, Monnens LA, Smeets HJ. Lemmink HH, et al. Among authors: brunner hg. Hum Mol Genet. 1994 Feb;3(2):317-22. doi: 10.1093/hmg/3.2.317. Hum Mol Genet. 1994. PMID: 8004101
Deafness, sensory neuropathy, and ovarian dysgenesis: a new syndrome or a broader spectrum of Perrault syndrome?
Linssen WH, Van den Bent MJ, Brunner HG, Poels PJ. Linssen WH, et al. Among authors: brunner hg. Am J Med Genet. 1994 May 15;51(1):81-2. doi: 10.1002/ajmg.1320510117. Am J Med Genet. 1994. PMID: 8030674
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