Hennekam RC - Search Results

1

Hutchinson-Gilford progeria syndrome: review of the phenotype.

Hennekam RC. Hennekam RC. Am J Med Genet A. 2006 Dec 1;140(23):2603-24. doi: 10.1002/ajmg.a.31346. Am J Med Genet A. 2006. PMID: 16838330 Review.

2

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.

3

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

4

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.

5

Further delineation of the 3-M syndrome with review of the literature.

Hennekam RC, Bijlsma JB, Spranger J. Hennekam RC, et al. Am J Med Genet. 1987 Sep;28(1):195-209. doi: 10.1002/ajmg.1320280127. Am J Med Genet. 1987. PMID: 3314510 Review.

6

Further delineation of the acro-renal-ocular syndrome.

Aalfs CM, van Schooneveld MJ, van Keulen EM, Hennekam RC. Aalfs CM, et al. Among authors: hennekam rc. Am J Med Genet. 1996 Mar 29;62(3):276-81. doi: 10.1002/(SICI)1096-8628(19960329)62:3<276::AID-AJMG14>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8882787

7

Autosomal dominant familial radial luxation, carpal fusion and scapular dysplasia with variable heart defects.

van Bever Y, Dijkstra PF, Hennekam RC. van Bever Y, et al. Among authors: hennekam rc. Am J Med Genet. 1996 Oct 28;65(3):213-7. doi: 10.1002/(SICI)1096-8628(19961028)65:3<213::AID-AJMG8>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 9240746

8

De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes.

Allanson JE, Hennekam RC, Ireland M. Allanson JE, et al. Among authors: hennekam rc. J Med Genet. 1997 Aug;34(8):645-50. doi: 10.1136/jmg.34.8.645. J Med Genet. 1997. PMID: 9279756 Free PMC article.

9

Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. III: primary field defects, sequences, and other complex anomalies.

Oostra RJ, Baljet B, Verbeeten BW, Hennekam RC. Oostra RJ, et al. Among authors: hennekam rc. Am J Med Genet. 1998 Oct 30;80(1):46-59. doi: 10.1002/(sici)1096-8628(19981102)80:1<46::aid-ajmg8>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9800911

10

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

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