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The clinical spectrum of type IV collagen mutations.
Lemmink HH, Schröder CH, Monnens LA, Smeets HJ. Lemmink HH, et al. Among authors: monnens la. Hum Mutat. 1997;9(6):477-99. doi: 10.1002/(SICI)1098-1004(1997)9:6<477::AID-HUMU1>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9195222 Review.
Genetic features of Alport's syndrome.
Schröder CH, Brunner H, Monnens LA. Schröder CH, et al. Among authors: monnens la. Contrib Nephrol. 1990;80:3-8. Contrib Nephrol. 1990. PMID: 2282819 Review. No abstract available.
Renal biopsy and family studies in 65 children with isolated hematuria.
Schröder CH, Bontemps CM, Assmann KJ, Schuurmans Stekhoven JH, Foidart JM, Monnens LA, Veerkamp JH. Schröder CH, et al. Among authors: monnens la. Acta Paediatr Scand. 1990 Jun-Jul;79(6-7):630-6. doi: 10.1111/j.1651-2227.1990.tb11527.x. Acta Paediatr Scand. 1990. PMID: 2386054
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