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1 xial and that of PHS is typically central or postaxial.
2 d as the cause of Miller (Genee-Weidemann or postaxial acrofacial dysostosis) syndrome (MIM 263750).
4 model in which Hoxd-12 promotes formation of postaxial chondrogenic condensations branching from this
5 , digits I and II forming earlier than their postaxial counterparts (digits III to V), a phenomenon k
7 me trans-animals show the growth of an extra postaxial digit VI, which is composed of a bony element
8 l lines of evidence indicate that posterior (postaxial) digit number in tetrapod vertebrates is const
10 3 knockdown in axolotl results in a shift to postaxial dominant limb skeleton formation, as well as e
14 ransgene was associated with marked pre- and postaxial limb defects, particularly in the hind limb, w
16 be fundamental to the shift from preaxial to postaxial polarity in formation of the tetrapod limb ske
18 syndrome comprising hydrometrocolpos (HMC), postaxial polydactyly (PAP) and congenital heart disease
19 ma syndrome (MKS) includes hydrometrocolpos, postaxial polydactyly and congenital heart disease, and
20 ia characterized by short limbs, short ribs, postaxial polydactyly and dysplastic nails and teeth.
22 eir offspring displayed a high penetrance of postaxial polydactyly and rib malformations not observed
25 ic linkage of the limb bud patterning defect postaxial polydactyly type A (designated PAP-A2, MIM 602
29 ormation of a supernumerary posterior digit (postaxial polydactyly), as well as cutaneous syndactyly
30 d to Meckel syndrome; the phenotype includes postaxial polydactyly, an ectopic digital defect hypothe
31 malformed limbs characterized by syndactyly, postaxial polydactyly, and dorsal transformations of ven
33 tal anomaly syndrome comprising mesoaxial or postaxial polydactyly, congenital heart disease and hydr
34 t) and generalized organomegaly, kinky tail, postaxial polydactyly, heart abnormalities, and edema.
35 (atrioventricular septal defect), skeleton (postaxial polydactyly, narrow chest, and shortening of l
36 use of limb malformations including pre- and postaxial polydactyly, Pallister-Hall syndrome and Greig
42 hepatic fibrosis, retinitis pigmentosa, and postaxial polydactyly; he harbors a de novo c.748G>C (p.