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Prenatal diagnosis of Meckel syndrome.
Fryns JP, Vandenberghe K, Van Assche FA, Cassiman JJ, van den Berghe H. Fryns JP, et al. Among authors: vandenberghe k. J Genet Hum. 1980 Dec;28(4):89-94. J Genet Hum. 1980. PMID: 7205201
Prenatal diagnosis of campomelic dwarfism.
Fryns JP, van den Berghe K, van Assche A, van den Berghe H. Fryns JP, et al. Clin Genet. 1981 Mar;19(3):199-201. doi: 10.1111/j.1399-0004.1981.tb00696.x. Clin Genet. 1981. PMID: 7273464 No abstract available.
Prenatal diagnosis in Belgium.
Vamos E, Vandenberghe K, Cassiman JJ. Vamos E, et al. Among authors: vandenberghe k. Eur J Hum Genet. 1997;5 Suppl 1:7-13. Eur J Hum Genet. 1997. PMID: 9101172
The fetal phenotype in 2p trisomy.
Fryns JP, Kleczkowska A, Moerman F, Van den Berghe K, Van den Berghe H. Fryns JP, et al. Ann Genet. 1986;29(4):269-71. Ann Genet. 1986. PMID: 3495231
The fetal phenotype in 15q2 duplication.
Fryns JP, Kleczkowska A, Moerman P, Vandenberghe K, Van den Berghe H. Fryns JP, et al. Among authors: vandenberghe k. Ann Genet. 1988;31(2):123-5. Ann Genet. 1988. PMID: 3261148
108 results