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Page 1
Mutations in NOTCH2 in families with Hajdu-Cheney syndrome.
Majewski J, Schwartzentruber JA, Caqueret A, Patry L, Marcadier J, Fryns JP, Boycott KM, Ste-Marie LG, McKiernan FE, Marik I, Van Esch H; FORGE Canada Consortium; Michaud JL, Samuels ME. Majewski J, et al. Among authors: marik i. Hum Mutat. 2011 Oct;32(10):1114-7. doi: 10.1002/humu.21546. Epub 2011 Sep 9. Hum Mutat. 2011. PMID: 21681853
Czech dysplasia metatarsal type: another type II collagen disorder.
Hoornaert KP, Marik I, Kozlowski K, Cole T, Le Merrer M, Leroy JG, Coucke PJ, Sillence D, Mortier GR. Hoornaert KP, et al. Among authors: marik i. Eur J Hum Genet. 2007 Dec;15(12):1269-75. doi: 10.1038/sj.ejhg.5201913. Epub 2007 Aug 29. Eur J Hum Genet. 2007. PMID: 17726487
[Historical aspects of bone dysplasias].
Marík I, Kuklík M. Marík I, et al. Cesk Pediatr. 1987 May;42(5):304-6. Cesk Pediatr. 1987. PMID: 3301014 Czech. No abstract available.
[Primary dysplastic ossification of the hip joints].
Marík I, Zeman J, Kuklík M. Marík I, et al. Acta Chir Orthop Traumatol Cech. 1984 Jun;51(3):241-7. Acta Chir Orthop Traumatol Cech. 1984. PMID: 6433608 Czech. No abstract available.
[Arthrogryposis multiplex congenita. I.].
Marík I, Schejbalová A, Kuklík M, Kraus J. Marík I, et al. Acta Chir Orthop Traumatol Cech. 1992;59(1):11-8. Acta Chir Orthop Traumatol Cech. 1992. PMID: 20429982 Czech.
[Arthrogryposis Multiplex Congenita - Part II.].
Marík I, Kuklík M, Kraus J, Schejbalová A, Kubát R. Marík I, et al. Acta Chir Orthop Traumatol Cech. 1992;59(2):67-76. Acta Chir Orthop Traumatol Cech. 1992. PMID: 20483061 Czech.
40 results