Moerman P - Search Results

1

MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomalies.

Witters I, Devriendt K, Spinnewijn D, Moerman P, Van Assche FA, Fryns JP. Witters I, et al. Among authors: moerman p. Am J Med Genet. 2002 Jan 22;107(3):233-6. doi: 10.1002/ajmg.10131. Am J Med Genet. 2002. PMID: 11807905

2

Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses.

Witters I, Moerman P, Fryns JP. Witters I, et al. Among authors: moerman p. Am J Med Genet. 2002 Nov 15;113(1):23-8. doi: 10.1002/ajmg.10698. Am J Med Genet. 2002. PMID: 12400062

3

Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler type.

Witters I, Moerman P, Devriendt K, Braet P, Van Schoubroeck D, Van Assche FA, Fryns JP. Witters I, et al. Among authors: moerman p. Am J Med Genet. 2002 Feb 15;108(1):41-4. Am J Med Genet. 2002. PMID: 11857548

4

Multiple congenital anomalies syndrome with multicystic renal dysplasia, postaxial polydactyly and lumbosacral meningocoele. Difficulties in nosological classification and genetic counseling.

Witters I, Moerman P, Natens R, Van Assche FA, Fryns JP. Witters I, et al. Among authors: moerman p. Genet Couns. 2002;13(2):147-9. Genet Couns. 2002. PMID: 12150214

5

Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome.

Petit P, Moerman P, Fryns JP. Petit P, et al. Among authors: moerman p. Am J Med Genet. 1992 Feb 1;42(3):343-5. doi: 10.1002/ajmg.1320420318. Am J Med Genet. 1992. PMID: 1536176

6

Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformations.

Petit P, Moerman P, Fryns JP. Petit P, et al. Among authors: moerman p. Clin Genet. 1992 Apr;41(4):175-7. doi: 10.1111/j.1399-0004.1992.tb03658.x. Clin Genet. 1992. PMID: 1576753

7

Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlap.

Moerman P, Fryns JP, Vandenberghe K, Lauweryns JM. Moerman P, et al. Am J Med Genet. 1992 Feb 15;42(4):470-9. doi: 10.1002/ajmg.1320420412. Am J Med Genet. 1992. PMID: 1609831

8

Pathogenesis of the lethal multiple pterygium syndrome.

Moerman P, Fryns JP, Cornelis A, Bergmans G, Vandenberghe K, Lauweryns JM. Moerman P, et al. Am J Med Genet. 1990 Mar;35(3):415-21. doi: 10.1002/ajmg.1320350319. Am J Med Genet. 1990. PMID: 2309791

9

Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.

Fryns JP, Moerman P. Fryns JP, et al. Among authors: moerman p. J Med Genet. 1988 Jul;25(7):498-9. doi: 10.1136/jmg.25.7.498. J Med Genet. 1988. PMID: 3172145 Free PMC article.

10

Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation.

Legius E, Moerman P, Fryns JP, Vandenberghe K, Eggermont E. Legius E, et al. Among authors: moerman p. Am J Med Genet. 1988 Oct;31(2):269-72. doi: 10.1002/ajmg.1320310203. Am J Med Genet. 1988. PMID: 3232694

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