ライフサイエンスコーパス: autosomally

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1 We discuss how an autosomally associated HMT may participate in silencing

2 e, in which the male phenotype is controlled autosomally by the Ods mutation.

3 e lineage across numerous linguistically and autosomally divergent populations have previously been u

4 s in the etiology of a number of undiagnosed autosomally dominant cases of amelogenesis imperfecta.

5 aryngeal muscular dystrophy is a late-onset, autosomally dominant disorder characterized by progressi

6 Tuberous sclerosis (TSC) is an autosomally dominant neurocutaneous disease notable for

7 tumors arising in such families exhibited an autosomally dominant pattern of inheritance.

8 The inheritance pattern is apparently autosomally dominant with a segregation ratio of 40.1% f

9 Min mice have an autosomally dominantly inherited predisposition to multi

10 Both neurogenic and myopathic forms of autosomally dominantly inherited scapuloperoneal syndrom

11 tive, specific for an HLA class I-restricted autosomally encoded minor H Ag, but was only weakly cyto

12 ar titration between an X-encoded RNA and an autosomally encoded protein dictates Xist induction.

13 osome genes, but both show homology to known autosomally encoded proteins.

14 on the X, but surprisingly XND-1 protein is autosomally enriched.

15 A new, autosomally inherited abnormal fibrinogen associated wit

16 Willebrand disease (VWD) is the most common autosomally inherited bleeding disorder.

17 ) or branched-chain alpha-ketoaciduria is an autosomally inherited disorder in the catabolism of bran

18 Tuberous sclerosis complex (TSC) is an autosomally inherited disorder that causes tumors to for

19 von Willebrand disease (vWD) is a common, autosomally inherited, bleeding disorder caused by quant

20 h a cosmid-based transgene that serves as an autosomally linked duplication of a small region of the

21 her confirmed by combination of X-linked and autosomally located miniwhite reporter genes in metafema

22 t in the male germline, so expression of the autosomally located spe-5 gene ensures that a V-ATPase B

23 n our search for the disease gene underlying autosomally recessively inherited infantile onset spinoc

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