Hennekam RC - Search Results

1

A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability.

Cobben JM, Weiss MM, van Dijk FS, De Reuver R, de Kruiff C, Pondaag W, Hennekam RC, Yntema HG. Cobben JM, et al. Among authors: hennekam rc. Eur J Med Genet. 2014 Nov-Dec;57(11-12):636-8. doi: 10.1016/j.ejmg.2014.09.002. Epub 2014 Sep 30. Eur J Med Genet. 2014. PMID: 25281490

2

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.

3

Acquired alopecia, mental retardation, short stature, microcephaly, and optic atrophy.

Hennekam RC, Renckens-Wennen EG. Hennekam RC, et al. J Med Genet. 1990 Oct;27(10):635-6. doi: 10.1136/jmg.27.10.635. J Med Genet. 1990. PMID: 2246773 Free PMC article.

4

Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation.

Hennekam RC, Geerdink RA, Hamel BC, Hennekam FA, Kraus P, Rammeloo JA, Tillemans AA. Hennekam RC, et al. Among authors: hennekam fa. Am J Med Genet. 1989 Dec;34(4):593-600. doi: 10.1002/ajmg.1320340429. Am J Med Genet. 1989. PMID: 2624276

5

Further delineation of the Yunis-Varon syndrome.

Hennekam RC, Vermeulen-Meiners C. Hennekam RC, et al. J Med Genet. 1989 Jan;26(1):55-8. doi: 10.1136/jmg.26.1.55. J Med Genet. 1989. PMID: 2918527 Free PMC article.

6

Haspeslagh syndrome without severe mental retardation and pterygia?

van Bever Y, Hennekam RC. van Bever Y, et al. Among authors: hennekam rc. Clin Genet. 1995 May;47(5):263-6. doi: 10.1111/j.1399-0004.1995.tb04308.x. Clin Genet. 1995. PMID: 7554353

7

Clinical profile of Angelman syndrome at different ages.

Buntinx IM, Hennekam RC, Brouwer OF, Stroink H, Beuten J, Mangelschots K, Fryns JP. Buntinx IM, et al. Among authors: hennekam rc. Am J Med Genet. 1995 Mar 27;56(2):176-83. doi: 10.1002/ajmg.1320560213. Am J Med Genet. 1995. PMID: 7625442

8

18q- and 18q+ mosaicism in a mentally retarded boy.

Ausems MG, Bhola SL, Post-Blok CA, Hennekam RC, de France HF. Ausems MG, et al. Among authors: hennekam rc. Am J Med Genet. 1994 Nov 15;53(3):296-9. doi: 10.1002/ajmg.1320530317. Am J Med Genet. 1994. PMID: 7856666

9

Spastic paraplegia, dysarthria, brachydactyly, and cone shaped epiphyses: confirmation of the Fitzsimmons syndrome.

Hennekam RC. Hennekam RC. J Med Genet. 1994 Mar;31(3):251-2. doi: 10.1136/jmg.31.3.251. J Med Genet. 1994. PMID: 8014978 Free PMC article.

10

Johnson-McMillin syndrome: report of another family.

Hennekam RC, Holtus FJ. Hennekam RC, et al. Am J Med Genet. 1993 Oct 1;47(5):714-6. doi: 10.1002/ajmg.1320470526. Am J Med Genet. 1993. PMID: 8267002 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

595 results

Search Page

Filters