van der Hagen CB - Search Results

1

Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study Group.

Gedde-Dahl T Jr, Trygstad O, Van Maldergem L, Magré J, van der Hagen CB, Olaisen B, Stenersen M, Mevåg B. Gedde-Dahl T Jr, et al. Among authors: van maldergem l, van der hagen cb. Acta Paediatr Suppl. 1996 Jun;413:52-8. doi: 10.1111/j.1651-2227.1996.tb14266.x. Acta Paediatr Suppl. 1996. PMID: 8783773

2

Hereditary pituitary dwarfism with spontaneous puberty.

Seip M, Van Der Hagen CB, Trygstad O. Seip M, et al. Among authors: van der hagen cb. Arch Dis Child. 1968 Feb;43(227):47-52. doi: 10.1136/adc.43.227.47. Arch Dis Child. 1968. PMID: 5642983 Free PMC article. No abstract available.

3

Registration of Down syndrome in the Medical Birth Registry of Norway: validity and time trends.

Melve KK, Lie RT, Skjaerven R, Van Der Hagen CB, Gradek GA, Jonsrud C, Braathen GJ, Irgens LM. Melve KK, et al. Among authors: van der hagen cb. Acta Obstet Gynecol Scand. 2008;87(8):824-30. doi: 10.1080/00016340802217184. Acta Obstet Gynecol Scand. 2008. PMID: 18607831 Free article.

4

Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40-year-old woman with a mosaic Turner's karyotype (45,X/47,XXX).

Acharya G, Jonsrud C, van der Hagen C, Maltau JM. Acharya G, et al. Acta Obstet Gynecol Scand. 2003 Aug;82(8):773-4. doi: 10.1034/j.1600-0412.2003.00071.x. Acta Obstet Gynecol Scand. 2003. PMID: 12848653 Free article. No abstract available.

5

A partial trisomy 1q patient with a deletion 1q22 and an insertion 1(q42q44) into 1q22.

Misceo D, Rocchi M, van der Hagen CB, Frengen E. Misceo D, et al. Among authors: van der hagen cb. Am J Med Genet A. 2009 Feb;149A(2):290-3. doi: 10.1002/ajmg.a.32623. Am J Med Genet A. 2009. PMID: 19161140 Review. No abstract available.

6

A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient.

Misceo D, Bjørgo K, Ormerod E, Ringen Ø, Rocchi M, van der Hagen CB, Frengen E. Misceo D, et al. Among authors: van der hagen cb. Am J Med Genet A. 2008 Dec 15;146A(24):3230-3. doi: 10.1002/ajmg.a.32582. Am J Med Genet A. 2008. PMID: 19012337 No abstract available.

7

[A hereditary abnormality as paternity evidence].

van der Hagen CB. van der Hagen CB. Tidsskr Nor Laegeforen. 2007 Jun 28;127(13):1817. Tidsskr Nor Laegeforen. 2007. PMID: 17599157 Free article. Norwegian. No abstract available.

8

Follow-up of a girl with cleft lip and palate and multiple malformations: trisomy 20 mosaicism.

Strømme P, van der Hagen CB, Haakonsen M, Risberg K, Hennekam R. Strømme P, et al. Among authors: van der hagen cb. Scand J Plast Reconstr Surg Hand Surg. 2005;39(3):178-9. doi: 10.1080/02844310510006141. Scand J Plast Reconstr Surg Hand Surg. 2005. PMID: 16019751

9

A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2.

Kjaer KW, Eiberg H, Hansen L, van der Hagen CB, Rosendahl K, Tommerup N, Mundlos S. Kjaer KW, et al. Among authors: van der hagen cb. J Med Genet. 2006 Mar;43(3):225-31. doi: 10.1136/jmg.2005.034058. Epub 2005 Jul 13. J Med Genet. 2006. PMID: 16014698 Free PMC article.

10

An excess of chromosome 1 breakpoints in male infertility.

Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N. Bache I, et al. Among authors: van der hagen cb. Eur J Hum Genet. 2004 Dec;12(12):993-1000. doi: 10.1038/sj.ejhg.5201263. Eur J Hum Genet. 2004. PMID: 15367911

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