CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens.
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How is the Human Genome Project doing, and what have we learned so far?CFTR Gene Mutations and Asthma in Indian Children: A Case-Control Study.The molecular basis of partial penetrance of splicing mutations in cystic fibrosis.Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis.Asthma and pulmonary function abnormalities in heterozygotes for cystic fibrosis transmembrane regulator gene mutations.
P2860
CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens.
description
1995 nî lūn-bûn
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1995年の論文
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name
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@ast
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@en
type
label
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@ast
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@en
prefLabel
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@ast
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@en
P2093
P2860
P1476
CFTR haplotype analysis reveal ...... l aplasia of the vas deferens.
@en
P2093
Brautbar C
Levinson D
Nissim-Rafinia M
Rave-Harel N
P2860
P304
P407
P577
1995-06-01T00:00:00Z