Delfortrie J - Search Results

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Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.

Lapière JC, Verloes A, Herens C, Delfortrie J, Van Maldergem L, Gillerot Y, Koulischer L. Lapière JC, et al. Among authors: delfortrie j. Genet Couns. 1992;3(3):155-9. Genet Couns. 1992. PMID: 1388935

Male pseudohermaphroditism with persistent müllerian structures, mental retardation and Borjeson-Forssman-Lehmann-like features: a new syndrome?

Verloes A, Gillerot Y, Delfortrie J, Zeevaert-Arnold MT, Collard R, Koulischer L, Fryns JP. Verloes A, et al. Among authors: delfortrie j. Genet Couns. 1990;1(3-4):219-25. Genet Couns. 1990. PMID: 2098045

GOMBO syndrome of growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia: a possible "new" recessively inherited MCA/MR syndrome.

Verloes A, Delfortrie J, Lambotte C. Verloes A, et al. Among authors: delfortrie j. Am J Med Genet. 1989 Jan;32(1):15-8. doi: 10.1002/ajmg.1320320104. Am J Med Genet. 1989. PMID: 2705477 No abstract available.

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