van den Berghe H - Search Results

1

Fryns JP, Macken J, Vinken L, Igodt-Ameye L, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1978 Jun 9;42(2):129-35. doi: 10.1007/BF00283632. Hum Genet. 1978. PMID: 669698

2

Ring chromosome 15 syndrome.

Fryns JP, Timmermans J, Hondt FD, François B, Emmery L, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1979 Sep 2;51(1):43-8. doi: 10.1007/BF00278290. Hum Genet. 1979. PMID: 500090

3

Familial occurrence of severe ulnar aplasia and lobster claw feet: a new syndrome.

van den Berghe H, Dequeker J, Fryns JP, David G. van den Berghe H, et al. Hum Genet. 1978 May 16;42(1):109-13. doi: 10.1007/BF00291633. Hum Genet. 1978. PMID: 565745

4

The Coffin syndrome.

Fryns JP, Vinken L, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1977 May 10;36(3):271-6. doi: 10.1007/BF00446276. Hum Genet. 1977. PMID: 852873

5

Down's syndrome in brother and sister without evident trisomy 21.

Parloir C, Fryns JP, Van den Berghe H. Parloir C, et al. Among authors: van den berghe h. Hum Genet. 1979 Oct 1;51(2):227-30. doi: 10.1007/BF00287182. Hum Genet. 1979. PMID: 159858

6

A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities.

Fryns JP, Moerman F, Goddeeris P, Bossuyt C, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1979;50(1):65-70. doi: 10.1007/BF00295591. Hum Genet. 1979. PMID: 381161

7

Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).

Fryns JP, Casaer P, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1979 Jan 25;46(2):237-41. doi: 10.1007/BF00291927. Hum Genet. 1979. PMID: 422207

8

Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis.

Fryns JP, Van Den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1979 Jan 19;46(1):21-7. doi: 10.1007/BF00278898. Hum Genet. 1979. PMID: 429003

9

Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype.

Fryns JP, Vinken L, Marien J, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1979 Feb 15;46(3):341-4. doi: 10.1007/BF00273319. Hum Genet. 1979. PMID: 437778

10

Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.

Fryns JP, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Hum Genet. 1979 Mar 12;47(2):213-6. doi: 10.1007/BF00273205. Hum Genet. 1979. PMID: 437787

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