van Essen AJ - Search Results

1

Renal defects and limb deficiencies in 197 infants: is it possible to define the "acrorenal syndrome"?

Kroes HY, Olney RS, Rosano A, Liu Y, Castilla EE, Cocchi G, De Vigan C, Martínez-Frías ML, Mastroiacovo P, Merlob P, Mutchinick O, Ritvanen A, Stoll C, van Essen AJ, Cobben JM, Cornel MC. Kroes HY, et al. Among authors: van essen aj. Am J Med Genet A. 2004 Aug 30;129A(2):149-55. doi: 10.1002/ajmg.a.30176. Am J Med Genet A. 2004. PMID: 15316969

2

Comparison of couples referred and not referred for genetic counseling in a genetic clinic after the birth of a child with a congenital anomaly: a study in a population in the northeastern Netherlands.

Cornel MC, van Essen AJ, ten Kate LP. Cornel MC, et al. Among authors: van essen aj. Am J Med Genet. 1992 Feb 1;42(3):387-92. doi: 10.1002/ajmg.1320420329. Am J Med Genet. 1992. PMID: 1536186

3

Ectrodactyly with fibular aplasia: a separate entity?

Menke LA, Bijlsma EK, van Essen AJ, van den Boogaard MJ, van Rijn RR, Cobben JM. Menke LA, et al. Among authors: van essen aj, van den boogaard mj, van rijn rr. Eur J Med Genet. 2008 Sep-Oct;51(5):488-96. doi: 10.1016/j.ejmg.2008.04.001. Epub 2008 May 2. Eur J Med Genet. 2008. PMID: 18547886

4

A boy with Poland anomaly and facio-auriculo-vertebral dysplasia.

Cobben JM, van Essen AJ, McParland PC, Polman HA, ten Kate LP. Cobben JM, et al. Among authors: van essen aj. Clin Genet. 1992 Feb;41(2):105-7. doi: 10.1111/j.1399-0004.1992.tb03643.x. Clin Genet. 1992. PMID: 1544210

5

Poland anomaly in mother and daughter.

Cobben JM, Robinson PH, van Essen AJ, van der Wiel HL, ten Kate LP. Cobben JM, et al. Among authors: van essen aj, van der wiel hl. Am J Med Genet. 1989 Aug;33(4):519-21. doi: 10.1002/ajmg.1320330423. Am J Med Genet. 1989. PMID: 2556920

6

Two cases of the caudal duplication anomaly including a discordant monozygotic twin.

Kroes HY, Takahashi M, Zijlstra RJ, Baert JA, Kooi KA, Hofstra RM, van Essen AJ. Kroes HY, et al. Among authors: van essen aj. Am J Med Genet. 2002 Nov 1;112(4):390-3. doi: 10.1002/ajmg.10594. Am J Med Genet. 2002. PMID: 12376942

7

Ehlers-Danlos syndrome type IV: unusual congenital anomalies in a mother and son with a COL3A1 mutation and a normal collagen III protein profile.

Kroes HY, Pals G, van Essen AJ. Kroes HY, et al. Among authors: van essen aj. Clin Genet. 2003 Mar;63(3):224-7. doi: 10.1034/j.1399-0004.2003.00047.x. Clin Genet. 2003. PMID: 12694234

8

Malpuech syndrome: three patients and a review.

Kerstjens-Frederikse WS, Brunner HG, van Dael CM, van Essen AJ. Kerstjens-Frederikse WS, et al. Among authors: van essen aj, van dael cm. Am J Med Genet A. 2005 May 1;134(4):450-3. doi: 10.1002/ajmg.a.30662. Am J Med Genet A. 2005. PMID: 15793834 Review.

9

Referral for genetic counseling after the birth of a child with a congenital anomaly in the Northern Netherlands.

Sikkens EH, de Walle HE, Reefhuis J, van Tintelen JP, van Essen AJ. Sikkens EH, et al. Among authors: van essen aj, van tintelen jp. Am J Med Genet. 2002 Oct 1;112(2):133-7. doi: 10.1002/ajmg.10680. Am J Med Genet. 2002. PMID: 12244545

10

Perlman syndrome: four additional cases and review.

Henneveld HT, van Lingen RA, Hamel BC, Stolte-Dijkstra I, van Essen AJ. Henneveld HT, et al. Among authors: van essen aj, van lingen ra. Am J Med Genet. 1999 Oct 29;86(5):439-46. Am J Med Genet. 1999. PMID: 10508986 Review.

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