ectodermal造句
1) Hypohydrotic ectodermal dysplasia is a common group of hereditary diseases, with congenital tooth loss as the predominant oral symptom.
2) Ectodermal dysplasia(ED)is an X-linked inherited disease. The most common is the hypohidrotic X-linked form affecting male subjects.
3) We derived cell populations with properties of ectodermal and mesenchymal cells in 2D culture and incorporated these divergent cell populations into 3D epithelial tissues.
4) Ectodermal skin muscle cells in myofibril generally arranged along the axis of the body, the contraction of the body shorter.
5) The fore-gut and hind-gut are of ectodermal origin and the mid-gut arises from endoderm.
6) Objective To study clinical and genetic features of hidrotic ectodermal dysplasia (HED) in Chinese.
7) Mesodermal-type bones, muscles, connective tissue, fulfilling the patient, physical type than the ectodermal thin people get sick more delicate.
8) CFC syndrome and CS can be distinguished from NS by the presence of ectodermal abnormalities, mental retardation and a lack of familial cases.
9) Similar sequential and reciprocal interactions between the epithelium and mesenchyme regulate the early steps of development in all ectodermal organs.
10) Objective To identify the mutations of ED 1 gene in a family with X - linked hypohidrotic ectodermal dysplasia.
11) The inner ear, which mediates hearing and equilibrium, develops from an ectodermal placode located adjacent to the developing hindbrain.
12) ABSTRACT:Objective To identify the mutations of ED1 gene in a family with X-linked hypohidrotic ectodermal dysplasia.
13) Objective To analyze genetic types and clinical features with anhidrotic ectodermal dysplasia ( EDA ).
14) Objetive : To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.
15) Objective To detect ED1 gene mutations in the families with X-linked hypohidrotic ectodermal dysplasia (XLHED).
16) Objective: To study the complete dentures for children with hypohidrotic ectodermal dysphasia .
17) Objective : To detect ED 1 gene mutation in three hypohidrotic ectodermal dysplasia ( HED ) nuclear families.