x-linked造句
1 It is compatible with the X-linked recessive inheritance.
2 Ectodermal dysplasia(ED)is an X-linked inherited disease. The most common is the hypohidrotic X-linked form affecting male subjects.
3 As an X-linked condition, choroideremia usually affects men, leading to severe vision loss or blindness in middle age.
4 Objective To improve the recognition and diagnosis of X-linked hypophosphatemia (XLH).
5 Two main modes of inheritance exist: X-linked and autosomal dominant.
6 Hemophilia B is an X-linked bleeding disorder caused by the deficiency of clotting factor IX (FIX).
7 Medically, the condition is called X-linked Severe Combined Immunodeficiency (X-SCID).
8 Furthermore, the possibility for the development of LMO2-associated leukemia in patients with X-linked severe combined immunodeficiency after retroviral-mediated gene therapy was also discussed.
9 Inheriting Duchenne's or Becker's MD Duchenne's and Becker's muscular dystrophies are passed from mother to son through one of the mother's genes in a pattern called X-linked recessive inheritance.
10 Objective To investigate the clinical manifestations, diagnostic methods and treatment of X-linked agammaglobulinemia(XLA).
11 Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.
12 However, approximately 30% of IHH is familial and can be inherited in an autosomal dominant , autosomal recessive , or X-linked manner.
13 ABSTRACT:Objective To identify the mutations of ED1 gene in a family with X-linked hypohidrotic ectodermal dysplasia.
14 Objective To find a way of sampling without any wound and quick diagnosis of fetal sex and its application in X-linked recessive inheritance.
15 Sex-limited --- A trait that is expressed in only one sex, although the gene that determines the trait is not X-linked.
16 A variety of approaches have been used to address this issue, the most common of which is the study of tumors in women, who are heterozygous for X-linked marker enzymes.
17 Objective To detect ED1 gene mutations in the families with X-linked hypohidrotic ectodermal dysplasia (XLHED).
18 Conclusion: Mutations of ALD gene is the causes of X-linked recessive adrenoleukodystrophy in Chinese population.
19 There are several methods for sexing embryos, such as karyotype analysis, H-Y antigen detection, X-linked enzymatic determination and polymerase chain reaction (PCR) amplification.
20 The absence of ALAS2 leads to maturation arrest of primitive erythroid cells. Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia (XLSA).
21 Genetic analysis showed that the disease is inherited in X-linked recessive heredity. Female carriers have partial symptoms.
22 Objective To identity the ABCD1 gene mutation in a Chinese family with X-linked adrenoleukodystrophy(ALD).
23 Female mosaicism of the X chromosome has major implications for human health and disease and is the leading cause of female protection from X-linked genetic disorders.
24 The inheritance pattern of retinal disease in a specific breed might be dominant, recessive, or X-linked – a different gene.
25 In a new study, researchers propose that Henry had an X-linked genetic disorder and a rare blood type that could explain many of his problems.