ライフサイエンスコーパス: postaxial

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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).

3 al digit pattern and formation of additional postaxial cartilaginous condensations.

4 model in which Hoxd-12 promotes formation of postaxial chondrogenic condensations branching from this

5 me trans-animals show the growth of an extra postaxial digit VI, which is composed of a bony element

6 Forelimb defects, including postaxial ectrodactyly, metacarpal, and ulnar deficienci

7 The postaxial extra digit is also consistent with a role for

8 One of the mutations causes the postaxial hemimelia (px) phenotype, which consists of li

9 ransgene was associated with marked pre- and postaxial limb defects, particularly in the hind limb, w

10 NS and the limbs have 5 digits with an extra postaxial nubbin.

11 syndrome comprising hydrometrocolpos (HMC), postaxial polydactyly (PAP) and congenital heart disease

12 ma syndrome (MKS) includes hydrometrocolpos, postaxial polydactyly and congenital heart disease, and

13 ia characterized by short limbs, short ribs, postaxial polydactyly and dysplastic nails and teeth.

14 , hepatic biliary ductal plate malformation, postaxial polydactyly and polycystic kidneys.

15 eir offspring displayed a high penetrance of postaxial polydactyly and rib malformations not observed

16 Presence of postaxial polydactyly is suggestive of an underlying syn

17 phenotypic spectrum extending from isolated postaxial polydactyly to an EvC-like condition.

18 ic linkage of the limb bud patterning defect postaxial polydactyly type A (designated PAP-A2, MIM 602

19 e (GCPS), Pallister-Hall syndrome (PHS), and postaxial polydactyly type A (PAP-A).

20 In the forelimb autopod, pre- and postaxial polydactyly were found most commonly, but also

21 The Prx1(cre);Bmp4 mutants also had postaxial polydactyly with digit five duplications.

22 ormation of a supernumerary posterior digit (postaxial polydactyly), as well as cutaneous syndactyly

23 d to Meckel syndrome; the phenotype includes postaxial polydactyly, an ectopic digital defect hypothe

24 malformed limbs characterized by syndactyly, postaxial polydactyly, and dorsal transformations of ven

25 ition with dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature.

26 tal anomaly syndrome comprising mesoaxial or postaxial polydactyly, congenital heart disease and hydr

27 t) and generalized organomegaly, kinky tail, postaxial polydactyly, heart abnormalities, and edema.

28 use of limb malformations including pre- and postaxial polydactyly, Pallister-Hall syndrome and Greig

29 ysplasia, characterized by short stature and postaxial polydactyly.

30 epressed nasal bridge, frontal bossing), and postaxial polydactyly.

31 ed extensive limb soft tissue syndactyly and postaxial polydactyly.

32 red patterning of the forelimb, resulting in postaxial polydactyly.

33 e-induced mouse mutation displaying forelimb postaxial polysyndactyly.

34 When the postaxial talpid(2) limb bud (including all Shh-expressi

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