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REFERENCES Ahram, D., et al., 2009. A Homozygous Mutation In ADAMTSL4 Causes Autosomal-Recessive Isolated Ectopia Lentis. Am. J. Hum. Genet. 84, 274–278. Rangasetty and Karnath. Clinical Signs of Marfan Syndrome. p: 33–38. Hospital Physician. 2006. Van de Velde, S., Fillman, R., Yandow, S., 2006. Protrusio Acetabuli In Marfan Syndrome: History, Diagnosis, and Treatment. Journal Bone Joint Surg. Am. 88(3), 639–646. Faivre, L., et al., 2008. Contribution Of Molecular Analyses In Diagnosing Marfan Syndrome And Type I Fibrillinopathies: An International Study Of 1009 Probands. J. Med. Genet. 45, 384–390. Kumar, A. and Sarita Agarwal. 2014. Marfan Syndrome: An Eyesight Of Syndrome. Department of Genetics Institute of Medical Sciences. India. Mete Gene: 96-105. Loeys BL, Chen J, Neptune ER, et al. 2005. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2. Nat Genet. 37(3): 27581. Loeys BL et al. 2010. The Revised Ghent Nosology For The Marfan Syndrome. J Med Genet. 47:476-485. Pearson, D.G., et al., 2008. Report of the National Heart, Lung and Blood Institute and National Marfan Foundation

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REFERENCES

Ahram, D., et al., 2009. A Homozygous Mutation In ADAMTSL4 Causes Autosomal-

Recessive Isolated Ectopia Lentis. Am. J. Hum. Genet. 84, 274–278.

Rangasetty and Karnath. Clinical Signs of Marfan Syndrome. p: 33–38. Hospital Physician.

2006.

Van de Velde, S., Fillman, R., Yandow, S., 2006. Protrusio Acetabuli In Marfan Syndrome:

History, Diagnosis, and Treatment. Journal Bone Joint Surg. Am. 88(3), 639–646.

Faivre, L., et al., 2008. Contribution Of Molecular Analyses In Diagnosing Marfan

Syndrome And Type I Fibrillinopathies: An International Study Of 1009 Probands.

J. Med. Genet. 45, 384–390.

Kumar, A. and Sarita Agarwal. 2014. Marfan Syndrome: An Eyesight Of Syndrome.

Department of Genetics Institute of Medical Sciences. India. Mete Gene: 96-105.

Loeys BL, Chen J, Neptune ER, et al. 2005. A syndrome of altered cardiovascular,

craniofacial, neurocognitive and skeletal development caused by mutations in

TGFBR1 or TGFBR2. Nat Genet. 37(3): 27581.

Loeys BL et al. 2010. The Revised Ghent Nosology For The Marfan Syndrome. J Med

Genet. 47:476-485.

Pearson, D.G., et al., 2008. Report of the National Heart, Lung and Blood Institute and

National Marfan Foundation Working Group on Research in Marfan Syndrome and

Related Disorders. Circulation 118, 785–791.

The Marfan Foundation. 2012. A Guide to Marfan Syndrome and Related Disorders. CDC

Cooperative Agreement: USA.