van den Berghe H - Search Results

1

Prenatal diagnosis of homozygous familial hypercholesterolaemia. Expression of a genetic receptor disease in utero.

Brown MS, Kovanen PT, Goldstein JL, Eeckels R, Vandenberghe K, van den Berghe H, Fryns JP, Cassiman JJ. Brown MS, et al. Among authors: van den berghe h. Lancet. 1978 Mar 11;1(8063):526-9. doi: 10.1016/s0140-6736(78)90552-4. Lancet. 1978. PMID: 76071

2

Prenatal diagnosis of Meckel syndrome.

Fryns JP, Vandenberghe K, Van Assche FA, Cassiman JJ, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h, van assche fa. J Genet Hum. 1980 Dec;28(4):89-94. J Genet Hum. 1980. PMID: 7205201

3

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

4

Prenatal diagnosis of campomelic dwarfism.

Fryns JP, van den Berghe K, van Assche A, van den Berghe H. Fryns JP, et al. Among authors: van den berghe k, van den berghe h, van assche a. 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.

5

Growth hormone and lymphocyte transformation.

Vanderschueren-Lodeweyckx, Staf B, Van den Berghe H, Eggermont E, Eeckels R. Vanderschueren-Lodeweyckx, et al. Among authors: van den berghe h. Lancet. 1973 Feb 24;1(7800):441. doi: 10.1016/s0140-6736(73)90318-8. Lancet. 1973. PMID: 4119768 No abstract available.

6

The Roberts tetraphocomelia syndrome: identical limb defects in two siblings.

Fryns JP, Kleczkowska A, Moerman P, van den Berghe K, van den Berghe H. Fryns JP, et al. Among authors: van den berghe k, van den berghe h. Ann Genet. 1987;30(4):243-5. Ann Genet. 1987. PMID: 3501269

7

Familial paracentric inversion of the short arm of chromosome 3.

Fryns JP, van den Berghe H. Fryns JP, et al. Among authors: van den berghe h. Ann Genet. 1979;22(3):163-4. Ann Genet. 1979. PMID: 316673

8

Differences in agglutinability of adult and fetal human fibroblasts using phytohemagglutinin.

Cassiman JJ, David G, Van der Schueren B, Van Den Berghe H. Cassiman JJ, et al. Among authors: van der schueren b, van den berghe h. Cell Differ. 1977 Aug;6(2):133-45. doi: 10.1016/0045-6039(77)90035-5. Cell Differ. 1977. PMID: 560918

9

The fetal phenotype in 2p trisomy.

Fryns JP, Kleczkowska A, Moerman F, Van den Berghe K, Van den Berghe H. Fryns JP, et al. Among authors: van den berghe k, van den berghe h. Ann Genet. 1986;29(4):269-71. Ann Genet. 1986. PMID: 3495231

10

Quantitative assessment of the amount and the activity of trypsin associated with trypsinized cells.

Brugmans M, Cassiman JJ, Van Leuven F, Van den Berghe H. Brugmans M, et al. Among authors: van leuven f, van den berghe h. Cell Biol Int Rep. 1979 May;3(3):257-63. doi: 10.1016/0309-1651(79)90038-9. Cell Biol Int Rep. 1979. PMID: 445582

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

944 results

Search Page

Filters