Hennekam RC - Search Results

1

Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. IV: closure defects of the neural tube.

Oostra RJ, Baljet B, Hennekam RC. Oostra RJ, et al. Among authors: hennekam rc. Am J Med Genet. 1998 Oct 30;80(1):60-73. doi: 10.1002/(sici)1096-8628(19981102)80:1<60::aid-ajmg9>3.0.co;2-i. Am J Med Genet. 1998. PMID: 9800912

2

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.

3

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.

4

Rubinstein-Taybi syndrome in The Netherlands.

Hennekam RC, Van Den Boogaard MJ, Sibbles BJ, Van Spijker HG. Hennekam RC, et al. Am J Med Genet Suppl. 1990;6:17-29. doi: 10.1002/ajmg.1320370604. Am J Med Genet Suppl. 1990. PMID: 2118773

5

Historical study: Cornelia C. de Lange (1871-1950)--a pioneer in clinical genetics.

de Knecht-van Eekelen A, Hennekam RC. de Knecht-van Eekelen A, et al. Among authors: hennekam rc. Am J Med Genet. 1994 Sep 1;52(3):257-66. doi: 10.1002/ajmg.1320520302. Am J Med Genet. 1994. PMID: 7810555

6

Brachmann-de Lange syndrome "avant la lettre".

Oostra RJ, Baljet B, Hennekam RC. Oostra RJ, et al. Among authors: hennekam rc. Am J Med Genet. 1994 Sep 1;52(3):267-8. doi: 10.1002/ajmg.1320520303. Am J Med Genet. 1994. PMID: 7810556 No abstract available.

7

Bartsocas-Papas syndrome with internal anomalies: evidence for a more generalized epithelial defect or new syndrome?

Hennekam RC, Huber J, Variend D. Hennekam RC, et al. Am J Med Genet. 1994 Nov 1;53(2):102-7. doi: 10.1002/ajmg.1320530203. Am J Med Genet. 1994. PMID: 7856636

8

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.

9

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.

10

EEC syndrome and genitourinary anomalies: an update.

Maas SM, de Jong TP, Buss P, Hennekam RC. Maas SM, et al. Among authors: hennekam rc. Am J Med Genet. 1996 Jun 14;63(3):472-8. doi: 10.1002/(SICI)1096-8628(19960614)63:3<472::AID-AJMG11>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8737655 Review.

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