Merks JH - Search Results

1

Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups.

Maas SM, Vansenne F, Kadouch DJ, Ibrahim A, Bliek J, Hopman S, Mannens MM, Merks JH, Maher ER, Hennekam RC. Maas SM, et al. Among authors: merks jh. Am J Med Genet A. 2016 Sep;170(9):2248-60. doi: 10.1002/ajmg.a.37801. Epub 2016 Jul 15. Am J Med Genet A. 2016. PMID: 27419809

2

Phenotypic abnormalities: terminology and classification.

Merks JH, van Karnebeek CD, Caron HN, Hennekam RC. Merks JH, et al. Am J Med Genet A. 2003 Dec 15;123A(3):211-30. doi: 10.1002/ajmg.a.20249. Am J Med Genet A. 2003. PMID: 14608641

3

Neuroblastoma, maternal valproic acid use, in-vitro fertilization and family history of mosaic chromosome 22: coincidence or causal relationship?

Merks JH, Ceelie N, Caron HN, Hennekam RC. Merks JH, et al. Clin Dysmorphol. 2004 Jul;13(3):197-198. doi: 10.1097/01.mcd.0000123123.89795.fe. Clin Dysmorphol. 2004. PMID: 15194961

4

Prevalence of rib anomalies in normal Caucasian children and childhood cancer patients.

Merks JH, Smets AM, Van Rijn RR, Kobes J, Caron HN, Maas M, Hennekam RC. Merks JH, et al. Eur J Med Genet. 2005 Apr-Jun;48(2):113-29. doi: 10.1016/j.ejmg.2005.01.029. Epub 2005 Feb 12. Eur J Med Genet. 2005. PMID: 16053903

5

Normal values for morphological abnormalities in school children.

Merks JH, Ozgen HM, Cluitmans TL, van der Burg-van Rijn JM, Cobben JM, van Leeuwen FE, Hennekam RC. Merks JH, et al. Am J Med Genet A. 2006 Oct 1;140(19):2091-109. doi: 10.1002/ajmg.a.31355. Am J Med Genet A. 2006. PMID: 16838341

6

Prevalence and patterns of morphological abnormalities in patients with childhood cancer.

Merks JH, Ozgen HM, Koster J, Zwinderman AH, Caron HN, Hennekam RC. Merks JH, et al. JAMA. 2008 Jan 2;299(1):61-9. doi: 10.1001/jama.2007.66. JAMA. 2008. PMID: 18167407

7

Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.

Bliek J, Maas S, Alders M, Merks JH, Mannens M. Bliek J, et al. Among authors: merks jh. J Pediatr. 2008 Jul;153(1):95-100. doi: 10.1016/j.jpeds.2007.12.022. Epub 2008 Mar 7. J Pediatr. 2008. PMID: 18571544

8

Morphological abnormalities in children with thyroidal congenital hypothyroidism.

Kempers MJ, Ozgen HM, Vulsma T, Merks JH, Zwinderman KH, de Vijlder JJ, Hennekam RC. Kempers MJ, et al. Among authors: merks jh. Am J Med Genet A. 2009 May;149A(5):943-51. doi: 10.1002/ajmg.a.32777. Am J Med Genet A. 2009. PMID: 19367618

9

The face in congenital melanocytic nevus syndrome.

Kinsler V, Shaw AC, Merks JH, Hennekam RC. Kinsler V, et al. Among authors: merks jh. Am J Med Genet A. 2012 May;158A(5):1014-9. doi: 10.1002/ajmg.a.34217. Epub 2012 Mar 21. Am J Med Genet A. 2012. PMID: 22438093

10

PTEN hamartoma tumor syndrome and Gorham-Stout phenomenon.

Hopman SM, Van Rijn RR, Eng C, Bras J, Alders M, van der Horst CM, Hennekam RC, Merks JH. Hopman SM, et al. Among authors: merks jh. Am J Med Genet A. 2012 Jul;158A(7):1719-23. doi: 10.1002/ajmg.a.35406. Epub 2012 May 24. Am J Med Genet A. 2012. PMID: 22628360

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