Koulischer L - Search Results

1

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases.

Poncin J, Abs R, Velkeniers B, Bonduelle M, Abramowicz M, Legros JJ, Verloes A, Meurisse M, Van Gaal L, Verellen C, Koulischer L, Beckers A. Poncin J, et al. Among authors: koulischer l. Hum Mutat. 1999;13(1):54-60. doi: 10.1002/(SICI)1098-1004(1999)13:1<54::AID-HUMU6>3.0.CO;2-K. Hum Mutat. 1999. PMID: 9888389

2

New oral-acral syndrome with partial agenesis of the maxillary bones.

Verloes A, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Nov 15;44(5):605-7. doi: 10.1002/ajmg.1320440514. Am J Med Genet. 1992. PMID: 1481817

3

Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees.

Verloes A, Sakalihasan N, Koulischer L, Limet R. Verloes A, et al. Among authors: koulischer l. J Vasc Surg. 1995 Apr;21(4):646-55. doi: 10.1016/s0741-5214(95)70196-6. J Vasc Surg. 1995. PMID: 7707569 Free article.

4

Clinical overlap of Beckwith-Wiedemann, Perlman and Simpson-Golabi-Behmel syndromes: a diagnostic pitfall.

Verloes A, Massart B, Dehalleux I, Langhendries JP, Koulischer L. Verloes A, et al. Among authors: koulischer l. Clin Genet. 1995 May;47(5):257-62. doi: 10.1111/j.1399-0004.1995.tb04307.x. Clin Genet. 1995. PMID: 7554352

5

Pseudoaminopterin syndrome.

Verloes A, Bricteux G, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1993 Jun 1;46(4):394-7. doi: 10.1002/ajmg.1320460410. Am J Med Genet. 1993. PMID: 8357010 Review.

6

A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly.

Verloes A, Jamblin P, Koulischer L, Bourguignon JP. Verloes A, et al. Among authors: koulischer l. Clin Genet. 1996 Jan;49(1):2-5. doi: 10.1111/j.1399-0004.1996.tb04315.x. Clin Genet. 1996. PMID: 8721563 Free article.

7

Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).

Verloes A, Gillerot Y, Walczak E, Van Maldergem L, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Jan 15;42(2):180-3. doi: 10.1002/ajmg.1320420209. Am J Med Genet. 1992. PMID: 1733166 Review.

8

Genetic aspects of abdominal aortic aneurysm.

Verloes A, Sakalihasan N, Limet R, Koulischer L. Verloes A, et al. Among authors: koulischer l. Ann N Y Acad Sci. 1996 Nov 18;800:44-55. doi: 10.1111/j.1749-6632.1996.tb33297.x. Ann N Y Acad Sci. 1996. PMID: 8958981 Free article. Review. No abstract available.

9

Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?

Verloes A, Gillerot Y, Van Maldergem L, Schoos R, Herens C, Jamar M, Dideberg V, Lesenfants S, Koulischer L. Verloes A, et al. Among authors: koulischer l. Eur J Hum Genet. 2001 Jan;9(1):1-4. doi: 10.1038/sj.ejhg.5200575. Eur J Hum Genet. 2001. PMID: 11175292

10

Glaucoma-lens ectopia-microspherophakia-stiffness-shortness (GEMSS) syndrome: a dominant disease with manifestations of Weill-Marchesani syndromes.

Verloes A, Hermia JP, Galand A, Koulischer L, Dodinval P. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Sep 1;44(1):48-51. doi: 10.1002/ajmg.1320440112. Am J Med Genet. 1992. PMID: 1519650

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