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Aberrant twinning (diprosopus) associated with anencephaly.
Moerman P, Fryns JP, Goddeeris P, Lauweryns JM, Van Assche A. Moerman P, et al. Among authors: goddeeris p. Clin Genet. 1983 Oct;24(4):252-6. doi: 10.1111/j.1399-0004.1983.tb00079.x. Clin Genet. 1983. PMID: 6641001
Association of Meckel syndrome with M-anisosplenia in one patient.
Moerman P, Verbeken E, Fryns JP, Goddeeris P, Lauweryns JM. Moerman P, et al. Among authors: goddeeris p. Clin Genet. 1982 Sep;22(3):143-7. doi: 10.1111/j.1399-0004.1982.tb01425.x. Clin Genet. 1982. PMID: 7151299 No abstract available.
Full monosomy 21: a clinically recognizable syndrome?
Fryns JP, D'Hondt F, Goddeeris P, van den Berghe H. Fryns JP, et al. Among authors: goddeeris p. Hum Genet. 1977 Jun 30;37(2):155-9. doi: 10.1007/BF00393578. Hum Genet. 1977. PMID: 885536
Nonimmunologic hydrops fetalis. A study of ten cases.
Moerman P, Fryns JP, Goddeeris P, Lauweryns JM. Moerman P, et al. Among authors: goddeeris p. Arch Pathol Lab Med. 1982 Nov;106(12):635-40. Arch Pathol Lab Med. 1982. PMID: 6897172
54 results