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1 to abnormal somite differentiation and axial skeletal malformation.
2 es, alveolar bone hypoplasia, and a range of skeletal malformations.
3 and its application to the classification of skeletal malformations.
4 sents with disordered sexual development and skeletal malformations.
5 h multiple systemic abnormalities, including skeletal malformations.
6 morphia, short stature, cardiac defects, and skeletal malformations.
7 a mechanistic basis for most of the observed skeletal malformations.
8  malformations and 3.3 times greater risk of skeletal malformations.
9      COX-2 transgenic fetuses exhibit severe skeletal malformations and die shortly after birth.
10 or this mutation die at birth as a result of skeletal malformations and neural tube defects.
11 OP) is a rare autosomal dominant disorder of skeletal malformations and progressive extraskeletal oss
12  progressiva (FOP), a disorder of congenital skeletal malformations and progressive extraskeletal oss
13 terized by autosomal XY sex reversal, severe skeletal malformations and several craniofacial defects.
14 owth retardation, obesity, blepharophimosis, skeletal malformation, and increased serum lipid metabol
15 d clinical phenotypes including proteinuria, skeletal malformation, and neurological impairment.
16  include cystic kidneys, blindness, obesity, skeletal malformations, and other organ anomalies.
17                                              Skeletal malformations are localized along the entire ve
18  fetal malformations, especially cardiac and skeletal malformations at FPG levels >= 126 mg/dL [>= 7.
19                   Klippel-Feil syndrome is a skeletal malformation characterized by vertebral fusion.
20 s in increased chondrocyte proliferation and skeletal malformations consistent with the observed incr
21                                 Although the skeletal malformations did not phenocopy single or compo
22  increase in both occurrence and severity of skeletal malformations, extending from the craniocervica
23  shown to cause idiopathic short stature and skeletal malformations frequently observed in human pati
24    We show that the apoptosis and consequent skeletal malformations in acd mutants are dependent upon
25 gests that Cx40 deficiency accounts for many skeletal malformations in HOS and that Tbx5 regulation o
26 h mutations in FGF signaling molecules cause skeletal malformations in humans.
27 esponsible for the gametogenesis defects and skeletal malformations in the sks mice.
28  apoptosis is probably responsible for axial skeletal malformations in transgenic fetuses.
29  are reminiscent of the dominantly inherited skeletal malformation nail patella syndrome (NPS).
30 human motor neuropathies, arthropathies, and skeletal malformations of varying severity.
31 X9 gene cause campomelic dysplasia, a severe skeletal malformation syndrome associated with male-to-f
32    Campomelic dysplasia (CD) is a semilethal skeletal malformation syndrome with or without XY sex re
33 patients with campomelic dysplasia, a severe skeletal malformation syndrome, and the abundant express
34 cy results in campomelic dysplasia, a lethal skeletal malformation syndrome, and XY sex reversal.
35 (NICD) in the chondrocyte lineage results in skeletal malformations with decreased cartilage precurso
36                        The mutants also have skeletal malformations with fused vertebrae and ribs.
37 ion component, shared axial and appendicular skeletal malformations with Tbx5(+/Delta) mice.