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1 ynostosis, short stature, brachydactyly, and syndactyly).
2 al features and developmental delay, but not syndactyly.
3 to abnormal phalanges, fusion of sutures and syndactyly.
4 death, suggesting alternative mechanisms for syndactyly.
5 damts9 result in fully penetrant soft-tissue syndactyly.
6  may be a candidate gene for myopia and poly/syndactyly.
7 (GRHL3), and Grhl3(-/-)mice have soft-tissue syndactyly.
8 a causative gene for AM, pituitary, and poly/syndactyly.
9 l skeletal elements and profound soft-tissue syndactyly.
10 be a root cause of common syndromic forms of syndactyly.
11  CNS ventricular dilatation and two to three syndactyly.
12                            Neither child had syndactyly.
13 a with aberrant mesenteric blood supply, and syndactyly.
14 topods, missing phalanges and anterior digit syndactyly.
15 b-patterning defect in the form of bilateral syndactyly.
16 ydrocephalus, white spotting and soft tissue syndactyly.
17 ia, severe mental retardation, epilepsy, and syndactyly.
18 f several digits, and only minimal cutaneous syndactyly.
19 te to persistence of hyaloid vasculature and syndactyly.
20 ubepidermal blistering, cryptophthalmos, and syndactyly.
21  blood-filled blisters, cryptophthalmos, and syndactyly.
22 ons of all four feet, including polydactyly, syndactyly and brachydactylia.
23          The opposite trends for severity of syndactyly and cleft palate in relation to the two mutat
24                                              Syndactyly and cryptophthalmos in FS are sequelae of ski
25 , including alopecia, variable expression of syndactyly and hydrocephalus.
26 been associated with AM, sometimes with poly/syndactyly and hypopituitarism.
27 d limbs, leading additionally to soft tissue syndactyly and loss of wrist elements and phalanges due
28 ons of cleft lip, CLP, lip pits, skin-folds, syndactyly and oral adhesions which arise as the result
29 se mice developed extensive limb soft tissue syndactyly and postaxial polydactyly.
30 icant differences were found for severity of syndactyly and presence of cleft palate.
31 em disorder presenting with cryptophthalmos, syndactyly and renal defects and associated with loss-of
32 ormation usually comprising cryptophthalmos, syndactyly and renal defects.
33 malformation featuring mesomelic shortening, syndactyly and ventral nails (dorsal dimelia).
34  retardation, obesity, retinitis pigmentosa, syndactyly and/or polydactyly, short stature, and hypoge
35 e (exencephaly), failure of digit septation (syndactyly), and dysmorphogenesis of the placental labyr
36        Furthermore, fetuses had hemorrhages, syndactyly, and amputation of limbs, similar to human AB
37 oplantar hyperkeratosis and onychodysplasia, syndactyly, and cleft lip/cleft palate.
38 row nose, short palpebral fissures, type III syndactyly, and dental abnormalities including generaliz
39 ocephaly, pre- and postnatal growth failure, syndactyly, and distinctive facial features, including a
40 d genitourinary tract, including digit loss, syndactyly, and hypospadias.
41  characterized by cryptophthalmus, cutaneous syndactyly, and other malformations resulting from mutat
42 al malformations, including cryptophthalmos, syndactyly, and renal agenesis, which can lead to severe
43 postaxial polydactyly), as well as cutaneous syndactyly between all the digits.
44 MD and variable penetrance of brachydactyly, syndactyly, bone fragility, and learning disabilities.
45     Analysis of a large family with type III syndactyly, but atypical facial features, further sugges
46                The fusion of digits or toes, syndactyly, can be part of complex syndromes, including
47 uitin ligase lead to PNH associated with toe syndactyly, cleft palate and neurodevelopmental delay.
48 es, including hypertelorism, small mandible, syndactyly, clinodactyly, cleft palate, and scoliosis, w
49 efects, limb-reduction defects, polydactyly, syndactyly, diaphragmatic hernia, heart defects overall,
50                 The mutant mice also exhibit syndactyly (digit fusions) of the fore- and hindlimbs.
51                In addition, we show that the syndactyly documented in Sclerosteosis is present in bot
52 c disorder associated with long QT syndrome, syndactyly, dysmorphic features, and neurological sympto
53 polydactyly of the hindlimbs, and homozygous syndactyly ems (sne) animals are characterized by a fusi
54 play several developmental defects including syndactyly, facial dysmorphology, and a mild defect in h
55 der characterized by cardiac arrhythmias and syndactyly, highlighted roles for the L-type voltage-gat
56 der characterized by cardiac arrhythmias and syndactyly, highlighted unexpected roles for the L-type
57 ocessing by ADAMTS5, led to highly penetrant syndactyly in bt mice, suggesting that cleaved versican
58 enotypically variable expression that causes syndactyly in certain strains of cows.
59 p4 result in phenotypically similar forms of syndactyly in different mammalian species and that such
60  outside the "neonatal region" of Fbn2 cause syndactyly in mice.
61 gital cell death of mesenchymal cells causes syndactyly in multiple genetic mutants, Grhl3(-/-) embry
62  double mutation in FGFR2 was shown to cause syndactyly in the absence of craniosynostosis.
63 sting of 3/4 syndactyly in the hands and 4/5 syndactyly in the feet, with digit duplication in the sy
64 ngenital limb malformation consisting of 3/4 syndactyly in the hands and 4/5 syndactyly in the feet,
65 es, further suggested that isolated type III syndactyly is also located in this same region of the ge
66 e and small cartilaginous condensations, and syndactyly is associated with a complete absence of inte
67                                              Syndactyly is associated with a disorganized matrix, but
68 ck of interdigital cell death and associated syndactyly is related to an absence of interdigital cell
69 tral rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and apl
70 nted with severe global developmental delay, syndactyly of 2(nd) and 3(rd) toes, and severe muscle hy
71 olerance test and IQ=64, vaginal atresia and syndactyly of both feet).
72 ed mutation characterized by polydactyly and syndactyly of the forelimbs.
73 osis syndromes and is associated with severe syndactyly of the hands and feet and with central nervou
74          In Apert syndrome, characterised by syndactyly of the hands and feet, recurrent mutations of
75 mature fusion of cranial sutures) and severe syndactyly of the hands and feet.
76 characterized by craniosynostosis and severe syndactyly of the hands and feet.
77 Apert syndrome, characterized in addition by syndactyly of the limbs, involves specific mutations at
78 lation of the middle phalanges; the webbing (syndactyly) of the palm; the direction of the fibers of
79 lydactyly were found most commonly, but also syndactyly, oligodactyly, and abnormal digit placement a
80 nderlies phenotypes such as the accompanying syndactyly or craniofacial abnormalities in the majority
81  some cases; none had clinically significant syndactyly or deviation of the great toe.
82 normalities of the hands, ie, polydactyly or syndactyly or missing a hand digit.
83 dermal hemorrhagic blisters, renal agenesis, syndactyly or polydactyly and permanent fusion of eyelid
84  in HOXD13 have been associated with type II syndactyly or synpolydactyly, and, in HOXA13, with hand-
85 lity at E14-E17 associated with exencephaly, syndactyly, placentopathy, and kidney defects, all attri
86 ve severely malformed limbs characterized by syndactyly, postaxial polydactyly, and dorsal transforma
87 phaly and facial dysmorphism as well as foot syndactyly, renal agenesis, alopecia, iris coloboma, and
88 yonic epidermal blistering, cryptophthalmos, syndactyly, renal defects and a range of other developme
89 e disorder characterized by cryptophthalmos, syndactyly, renal defects, and a range of other developm
90 tion is allelic to the recessive shaker-with-syndactyly (sy) locus on chromosome 18.
91 pathways involved in the rare X-linked STAR (syndactyly, telecanthus and anogenital and renal malform
92 lopmental anomaly whose features include toe syndactyly, telecanthus, and anogenital and renal malfor
93 al patterning distinguish sm from many other syndactylies that result from later failure of cell deat
94                                              Syndactyly type III and conductive deafness can occur in
95                                          The syndactyly was more severe with the Pro253Arg mutation,
96                      All TS individuals have syndactyly (webbing of fingers and toes).
97               Overgrowths of soft tissue and syndactyly were also observed, resulting from impaired a
98 gital anomalies, including brachydactyly and syndactyly, were common.
99 al vessel number inhibited PCD, resulting in syndactyly, whereas an increment in vessel number and di
100                                     Type III syndactyly, which occurs as part of ODD, has also been r
101 ally characterized by 3/4 finger and 4/5 toe syndactyly with associated duplicated digits; hands and
102 ation defects (white belly spots) and simple syndactyly with high penetrance (>95%), and 24% of mutan
103 ism, colobomatous microphthalmia, ptosis and syndactyly with or without nephropathy, associated with

 
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