References

Akarsu AN, Akhan O, Sayli BS, Sayli U, Baskaya G, Sarfarazi M. A large Turkish kindred with syndactyly type II (synpoly-dactyly). 2. Homozygous phenotype? J Med Genet 1995; 32: 435-41

Bosse K, Betz RC, Lee Y-A, Wienker TF, Reis A, Kleen H, Propping P, Cichon S, Nothen MM. Localization of a gene for syndactyly type 1 to chromosome 2q34-q36. Am J Hum Genet 2000; 67: 492-7

Camera G, Camera A, Pozzolo S, Costa M, Mantero R. Synpoly-dactyly (type II syndactyly) with aplasia/hypoplasia of the middle phalanges of the toes: report on a family with eight affected members in four generations. Am J Med Genet 1995; 55: 244-6

Castilla EE, Paz JE, Orioli-Parreiras IM. Syndactyly: frequency of specific types. Am J Med Genet 1980; 5: 357-64

Cross HE, Lerberg DB, McKusick VA. Type II syndactyly. Am J Hum Genet 1968; 20: 368-80

David TJ, Winter RM. Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles. J Med Genet 1985; 22: 390-2

David TJ. Familial Poland anomaly. J Med Genet 1982; 19: 293-6

De Smet L, Mulier T, Fabry G. Syndactyly of the ring and small finger. Genet Couns 1994; 5:45-9 Fuhrmann W, Mosseler U, Neuss H. Zur Klinik und Genetik des Poland-Syndroms. Dtsch Med Wochenschr 1971; 96: 1076-8

Gillessen-Kaesbach G, Majewski F. Bilateral complete polysyn-

dactyly (type IV Haas).Am J Med Genet 1991; 38:29-31 Gladwin A, Donnai D, Metcalfe K, Schrander-Stumpel C, Brue-ton L, Verloes A, Aylsworth A, Toriello H, Winter R, Dixon M. Localization of a gene for oculodentodigital syndrome to human chromosome 6q22-q24. Hum Mol Genet 1997; 6: 123-7

Haas SL. Bilateral complete syndactylism of all fingers. Am J

Surg 1940; 50: 363-6 Kemp T, Ravn J. Über erbliche Hand-und Fussdeformitäten in einem 140-köpfigen Geschlecht, nebst einigen Bemerkungen über Poly- und Syndaktylie beim Menschen. Acta Psychiatr Neurol Scand 1932; 7: 275-96 Muragaki Y, Mundlos S, Upton J, Olsen BR. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science 1996; 272: 548-51 Offiah A, Hall CM. Radiological diagnosis of the constitutional disorders of bone. As easy as A, B, C? Pediatr Radiol 2003; 33:153-61

Opjordsmoen S, Nyberg-Hansen R. Hereditary spastic paraplegia with neurogenic bladder disturbances and syn-dactyly. Acta Neurol Scand 1980; 61:35-41 Rambaud-Cousson A, Dudin AA, Zuaiter AS, Thalji A. Syn-dactyly type IV/hexadactyly of feet associated with unilateral absence of the tibia. Am J Med Genet 1991; 40:144-5 Robinow M, Johnson GF, Broock GJ. Syndactyly type V. Am J

Med Genet 1982; 11: 475-82 Sarfarazi M,Akarsu AN, Sayli BS. Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker. Hum Mol Genet 1995; 4: 1453-8 Temtamy SA, McKusick VA. The genetics of hand malforma-

tions.Alan R Liss,New York, 1978 Thomsen O. Einige Eigentümlichkeiten der erblichen Poly-und Syndaktylie bei Menschen. Acta Med Scand 1927; 65: 609-44

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