Four half-siblings with infantile myofibromatosis... [Clin Genet. 2001] - PubMed

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Review Autosomal dominant inheritance of infantile myofibromatosis. [Am J Med Genet A. 2004]
Review Autosomal dominant inheritance of infantile myofibromatosis.
Zand DJ, Huff D, Everman D, Russell K, Saitta S, McDonald-McGinn D, Zackai EH. Am J Med Genet A. 2004 Apr 30; 126A(3):261-6.
Infantile myofibromatosis: two families supporting autosomal dominant inheritance. [Australas J Dermatol. 2011]
Infantile myofibromatosis: two families supporting autosomal dominant inheritance.
Smith A, Orchard D. Australas J Dermatol. 2011 Aug; 52(3):214-7. Epub 2011 Mar 1.
Infantile myofibromatosis: support for autosomal dominant inheritance. [J Am Acad Dermatol. 2003]
Infantile myofibromatosis: support for autosomal dominant inheritance.
Ikediobi NI, Iyengar V, Hwang L, Collins WE, Metry DW. J Am Acad Dermatol. 2003 Aug; 49(2 Suppl Case Reports):S148-50.
del(6)(q12q15) as the sole cytogenetic anomaly in a case of solitary infantile myofibromatosis. [Oncol Rep. 1999]
del(6)(q12q15) as the sole cytogenetic anomaly in a case of solitary infantile myofibromatosis.
Stenman G, Nadal N, Persson S, Gunterberg B, Angervall L. Oncol Rep. 1999 Sep-Oct; 6(5):1101-4.
Review Adams-Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant. [Am J Med Genet A. 2008]
Review Adams-Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant.
McGoey RR, Lacassie Y. Am J Med Genet A. 2008 Feb 15; 146A(4):488-91.

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Four half-siblings with infantile myofibromatosis: a case for autosomal-recessiv...
Four half-siblings with infantile myofibromatosis: a case for autosomal-recessive inheritance.
Clin Genet. 2001 Feb ;59(2):134-5.

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Essential role of the VirB machinery in the maturation of the Brucella abortus-containing vacuole.
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Pharmacokinetics of sabeluzole and dextromethorphan oxidation capacity in patien...
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Treatment of chronic granulomatous disease with nonmyeloablative conditioning an...
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Four half-siblings with infantile myofibromatosis: a case for autosomal-recessive inheritance.

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