Fryns JP - Search Results

1

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

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

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: fryns jp. Am J Med Genet. 2002 Nov 15;113(1):23-8. doi: 10.1002/ajmg.10698. Am J Med Genet. 2002. PMID: 12400062

3

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: fryns jp. Clin Genet. 1992 Apr;41(4):175-7. doi: 10.1111/j.1399-0004.1992.tb03658.x. Clin Genet. 1992. PMID: 1576753

4

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. Among authors: fryns jp. Am J Med Genet. 1992 Feb 15;42(4):470-9. doi: 10.1002/ajmg.1320420412. Am J Med Genet. 1992. PMID: 1609831

5

Pathogenesis of the lethal multiple pterygium syndrome.

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

6

[A new sublethal syndrome with multiple malformations associating diaphragmatic hernia, distal digital hypoplasia, and craniofacial anomalies. The "Fryns syndrome"].

Fryns JP, Moerman P, Van den Berghe H, Aymé S. Fryns JP, et al. J Genet Hum. 1989 Sep;37(3):203-5. J Genet Hum. 1989. PMID: 2625623 French.

7

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

Fryns JP, Moerman P. Fryns JP, et al. 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.

8

Suggestively increased rate of infant death in children of fra(X) positive mothers.

Fryns JP, Moerman P, Gilis F, d'Espallier L, Van den Berghe H. Fryns JP, et al. Am J Med Genet. 1988 May-Jun;30(1-2):73-5. doi: 10.1002/ajmg.1320300105. Am J Med Genet. 1988. PMID: 3177481

9

The pathology of trisomy 13 syndrome. A study of 12 cases.

Moerman P, Fryns JP, van der Steen K, Kleczkowska A, Lauweryns J. Moerman P, et al. Among authors: fryns jp. Hum Genet. 1988 Dec;80(4):349-56. doi: 10.1007/BF00273650. Hum Genet. 1988. PMID: 3198112

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: fryns jp. 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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