Vestermark S - Search Results

1

The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndrome.

Warburg M, Tommerup N, Vestermark S, Parving A, Weismann K, Russell B, Thomsen HK. Warburg M, et al. Among authors: vestermark s. Ophthalmic Paediatr Genet. 1990 Sep;11(3):201-7. doi: 10.3109/13816819009020980. Ophthalmic Paediatr Genet. 1990. PMID: 2280978

2

Aniridia and interstitial deletion of the short arm of chromosome 11.

Warburg M, Mikkelsen M, Andersen SR, Geertinger P, Larsen HW, Vestermark S, Parving A. Warburg M, et al. Among authors: vestermark s. Metab Pediatr Ophthalmol. 1980;4(2):97-102. Metab Pediatr Ophthalmol. 1980. PMID: 7442353 No abstract available.

3

Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case report.

Andersen SR, Geertinger P, Larsen HW, Mikkelsen M, Parving A, Vestermark S, Warburg M. Andersen SR, et al. Among authors: vestermark s. Ophthalmologica. 1977;176(3):171-7. doi: 10.1159/000308711. Ophthalmologica. 1977. PMID: 613291

4

[P 11 deletion syndrome. Aniridia, urogenital malformation and mental retardation].

Andersen SR, Geertinger P, Larsen HW, Mikkelsen M, Vestermark S, Warburg M. Andersen SR, et al. Among authors: vestermark s. Ugeskr Laeger. 1978 Aug 28;140(35):2112. Ugeskr Laeger. 1978. PMID: 211686 Danish. No abstract available.

5

The Hurler/Scheie phenotype in children from a consanguineous marriage: case report with electronmicroscopy of the conjunctiva and ERG.

Jensen OA, Pedersen C, Vestermark S, Warburg M. Jensen OA, et al. Among authors: vestermark s. Metab Pediatr Ophthalmol. 1980;4(3):133-4. Metab Pediatr Ophthalmol. 1980. PMID: 6779061 No abstract available.

6

Hurler/Scheie phenotype. Report of an inbred sibship with tapeto-retinal degeneration and electron-microscopie examination of the conjuctiva.

Jensen OA, Pedersen C, Schwartz M, Vestermark S, Warburg M. Jensen OA, et al. Among authors: vestermark s. Ophthalmologica. 1978;176(4):194-204. doi: 10.1159/000308739. Ophthalmologica. 1978. PMID: 96404

7

[Monosomy 21, G-deletion syndrome I, Anti-mongolism].

Vestermark S, Mikkelsen M. Vestermark S, et al. Ugeskr Laeger. 1974 Aug 12;136(33):1857. Ugeskr Laeger. 1974. PMID: 4280640 Danish. No abstract available.

8

Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.

Mikkelsen M, Vestermark S. Mikkelsen M, et al. Among authors: vestermark s. J Med Genet. 1974 Dec;11(4):389-93. doi: 10.1136/jmg.11.4.389. J Med Genet. 1974. PMID: 4140913 Free PMC article.

9

Fluorescein angiography in diabetic children.

Starup K, Larsen HW, Enk B, Vestermark S. Starup K, et al. Among authors: vestermark s. Acta Ophthalmol (Copenh). 1980 Jun;58(3):347-54. doi: 10.1111/j.1755-3768.1980.tb05733.x. Acta Ophthalmol (Copenh). 1980. PMID: 7415822

10

[18-trisomy syndrome. E-trisomy, Edwards' syndrome].

Niebuhr E, Vestermark S. Niebuhr E, et al. Among authors: vestermark s. Ugeskr Laeger. 1973 Mar 5;135(10):530. Ugeskr Laeger. 1973. PMID: 4698031 Danish. No abstract available.

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