van Essen AJ - Search Results

1

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

2

Unreported manifestations in two Dutch families with Bartsocas-Papas syndrome.

Veenstra-Knol HE, Kleibeuker A, Timmer A, ten Kate LP, van Essen AJ. Veenstra-Knol HE, et al. Among authors: van essen aj. Am J Med Genet A. 2003 Dec 15;123A(3):243-8. doi: 10.1002/ajmg.a.20308. Am J Med Genet A. 2003. PMID: 14608644 Review.

3

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

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

Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands.

van Essen AJ, Busch HF, te Meerman GJ, ten Kate LP. van Essen AJ, et al. Hum Genet. 1992 Jan;88(3):258-66. doi: 10.1007/BF00197256. Hum Genet. 1992. PMID: 1733827

6

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

7

An atypical case of Fanconi anemia in elderly sibs.

Kwee ML, van der Kleij JM, van Essen AJ, Begeer JH, Joenje H, Arwert F, ten Kate LP. Kwee ML, et al. Among authors: van essen aj, van der kleij jm. Am J Med Genet. 1997 Jan 31;68(3):362-6. Am J Med Genet. 1997. PMID: 9024573

8

The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.

van Essen AJ, Kneppers AL, van der Hout AH, Scheffer H, Ginjaar IB, ten Kate LP, van Ommen GJ, Buys CH, Bakker E. van Essen AJ, et al. Among authors: van der hout ah, van ommen gj. J Med Genet. 1997 Oct;34(10):805-12. doi: 10.1136/jmg.34.10.805. J Med Genet. 1997. PMID: 9350811 Free PMC article.

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

Duchenne muscular dystrophy inherited through paternal lines.

ten Kate LP, van Essen AJ. ten Kate LP, et al. Among authors: van essen aj. Am J Med Genet. 1992 Jan 15;42(2):214; author reply 215. doi: 10.1002/ajmg.1320420216. Am J Med Genet. 1992. PMID: 1733171 No abstract available.

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