28 related articles for article (PubMed ID: 2177188)
1. Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences.
Malik S; Girisha KM; Wajid M; Roy AK; Phadke SR; Haque S; Ahmad W; Koch MC; Grzeschik KH
BMC Med Genet; 2007 Dec; 8():78. PubMed ID: 18072967
[TBL] [Abstract][Full Text] [Related]
2. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract.
Goodman FR; Mundlos S; Muragaki Y; Donnai D; Giovannucci-Uzielli ML; Lapi E; Majewski F; McGaughran J; McKeown C; Reardon W; Upton J; Winter RM; Olsen BR; Scambler PJ
Proc Natl Acad Sci U S A; 1997 Jul; 94(14):7458-63. PubMed ID: 9207113
[TBL] [Abstract][Full Text] [Related]
3. [Genetic analysis of a Chinese pedigree with congenital synpolydactyly].
Qin W; Shu AL; Xing QH; Yang MS; Feng GY; He L
Yi Chuan Xue Bao; 2003 Oct; 30(10):973-7. PubMed ID: 14669516
[TBL] [Abstract][Full Text] [Related]
4. Synpolydactyly (type II syndactyly) with aplasia/hypoplasia of the middle phalanges of the toes: report on a family with eight affected members in four generations.
Camera G; Camera A; Pozzolo S; Costa M; Mantero R
Am J Med Genet; 1995 Jan; 55(2):244-6. PubMed ID: 7717427
[TBL] [Abstract][Full Text] [Related]
5. A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.
Sayli BS; Akarsu AN; Sayli U; Akhan O; Ceylaner S; Sarfarazi M
J Med Genet; 1995 Jun; 32(6):421-34. PubMed ID: 7666393
[TBL] [Abstract][Full Text] [Related]
6. The craniodigital syndrome of Scott: report of a second family.
Lorenz P; Hinkel GK; Hoffmann C; Rupprecht E
Am J Med Genet; 1990 Oct; 37(2):224-6. PubMed ID: 2174209
[TBL] [Abstract][Full Text] [Related]
7. Synpolydactyly in three generations of a Nigerian family.
Ofodile FA
East Afr Med J; 1982 Dec; 59(12):835-9. PubMed ID: 6307635
[No Abstract] [Full Text] [Related]
8. [Synpolydactyly: unusual features and variable expression in 5 generations of an Italian family].
Chessa Ricotti G; Lapi E; De Bernardi A; Corti P
Pediatr Med Chir; 1990; 12(3):259-63. PubMed ID: 2177188
[TBL] [Abstract][Full Text] [Related]
9. Type II familial synpolydactyly: report on two families with an emphasis on variations of expression.
Al-Qattan MM
Eur J Hum Genet; 2011 Jan; 19(1):112-4. PubMed ID: 20717165
[TBL] [Abstract][Full Text] [Related]
10. Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature.
Küster W; Lenz W; Kääriäinen H; Majewski F
Am J Med Genet; 1988 Sep; 31(1):99-115. PubMed ID: 3066221
[TBL] [Abstract][Full Text] [Related]
11. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
Gollop TR; Fontes LR
Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752
[TBL] [Abstract][Full Text] [Related]
12.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
