Koulischer L - Search Results

1

Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature.

Verloes A, Mulliez N, Gonzales M, Laloux F, Hermanns-Lê T, Piérard GE, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Jun 1;43(3):539-47. doi: 10.1002/ajmg.1320430308. Am J Med Genet. 1992. PMID: 1605246 Review.

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

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

4

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: review and delineation of the cerebro-acro-visceral early lethality (CAVE) multiplex syndrome.

Verloes A, Gillerot Y, Langhendries JP, Fryns JP, Koulischer L. Verloes A, et al. Among authors: koulischer l. Am J Med Genet. 1992 Jul 1;43(4):669-77. doi: 10.1002/ajmg.1320430404. Am J Med Genet. 1992. PMID: 1621756 Review.

5

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.

6

Monosomy 11q: report of two familial cases and review of the literature.

Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L. Hustinx R, et al. Among authors: koulischer l. Am J Med Genet. 1993 Sep 1;47(3):312-7. doi: 10.1002/ajmg.1320470303. Am J Med Genet. 1993. PMID: 8135272 Review.

7

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.

8

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.

9

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

10

Brachymorphism-onychodysplasia-dysphalangism syndrome.

Verloes A, Bonneau D, Guidi O, Berthier M, Oriot D, Van Maldergem L, Koulischer L. Verloes A, et al. Among authors: koulischer l. J Med Genet. 1993 Feb;30(2):158-61. doi: 10.1136/jmg.30.2.158. J Med Genet. 1993. PMID: 8445623 Free PMC article.

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