A large family with type IV radial polydactyly

Journal of Hand Surgery: European Volume

Volumn 23, Issue 4, 1998, Pages 530-533

  Seyhan, A ^a   Akarsu, N ^a   Keskin, F ^a  

^a CELAL BAYAR UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CRANIOFACIAL MALFORMATION; DISEASE CLASSIFICATION; FAMILY; HUMAN; PEDIGREE; POLYDACTYLY; SYNDACTYLY;

FINGERS; HAND DEFORMITIES, CONGENITAL; HUMANS; PEDIGREE; POLYDACTYLY; SYNDACTYLY; TOES;

EID: 0031876616     PISSN: 17531934     EISSN: 20436289     Source Type: Journal    
DOI: 10.1016/S0266-7681(98)80139-3     Document Type: Article

References (14)

1. Akarsu, AN, I Stoilov, E Yilmaz, BS Sayli, and M Sarfarazi (1996). Genomic structure of HOXD13 gene: A nine polyalanine duplication causes syndactyly in two unrelated families. Human Molecular Genetics, 5, 945-952.
2. Baraitser, M, RM Winter, and EM Brett (1983). Greig cephalopolysyndactyly: Report of 13 affected individuals in three families. Clinical Genetics, 24, 257-265.
3. Hentz, VR (1990). Congenital anomalies of the thumb. In JG Mc Carthy (Ed.), Plastic surgery, Vol. 8, 3rd edn (pp. 5106-5134). Philadelphia: WB Saunders.
4. Heutink, P, J Zguricas, and L van Oosterhout (1994). The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q. Nature Genetics, 6, 287-292.
5. Heutink, P, C Vermeij-Keers, and BA Oostra (1995). The genetic background of craniosynostosis syndromes. European Journal of Human Genetics, 3, 312-323.
6. Hollway, GE, GK Suthers, and EA Haan (1997). Mutation detection in FGFR2 craniosynostosis syndromes. Human Genetics, 99, 251-255.
7. Nicolai, JPA, and BCJ Hamel (1988). A family with complex bilateral polysyndactyly. Journal of Hand Surgery, 13A, 405-407.
8. Pettigrew, AL, F Greenberg, CT Caskey, and DH Ledbetter (1991). Greig syndrome associated with an interstitial deletion of 7p: Confirmation of the localization of Greig syndrome to 7pl3. Human Genetics, 87, 452-456.
9. Sarfarazi, M, AN Akarsu, and BS Sayli (1995). Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker. Human Molecular Genetics, 4, 1453-1458.
10. Sayli, BS, AN Akarsu, U Sayli, O Akhan, S Ceylaner, and M Sarfarazi (1995). A large Turkish kindred with syndactyly type II (synpolydactyly), 1: Field investigation, clinical and pedigree data. Journal of Medical Genetics, 32, 421-434.
11. Temtamy, SA, and VA McKusick (1978). The genetics of hand malformations. In D Bergsma (Ed.), Birth defects: original article series, Vol. XIV(3) (pp. 301-302). New York: Alan R Liss.
12. Tsukurov, O, A Boehmer, and J Flynn (1994). A complex bilateral polysyndactyly disease locus maps to chromosome 7q36. Nature Genetics, 6, 282-286.
13. Upton, J (1990). Congenital anomalies of the hand and forearm. In JG Mc Carthy (Ed.), Plastic surgery, Vol. 8, 3rd edn (pp. 5213-5398). Philadelphia: WB Saunders.
14. Vortkamp, A, M Gessler, and KH Grzeschik (1991). GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families. Nature, 352, 539-540.