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1 12 live births, including three infants with congenital abnormalities.
2 g an unprecedented epidemic linked to severe congenital abnormalities.
3 lar proliferation in situ did not reveal any congenital abnormalities.
4 -threatening infections and subsequent fetal congenital abnormalities.
5 terozygosity (AOH) in subjects with multiple congenital abnormalities.
6 far no definitive link between belimumab and congenital abnormalities.
7 cal deformities caused by trauma, tumors, or congenital abnormalities.
8 Opitz syndrome (SLOS) are born with multiple congenital abnormalities.
9 ue comprehensive views of cardiac valves and congenital abnormalities.
10 arr virus producing lymphoma, carcinoma, and congenital abnormalities.
11 eased risk for giving birth to children with congenital abnormalities.
12 ers constitute some of the most common human congenital abnormalities.
13 and management of infants with these common congenital abnormalities.
14 re perinatal outcomes, postnatal health, and congenital abnormalities.
15 ing causes of under-5 mortality in 2015 were congenital abnormalities (35 700 deaths, 95% uncertainty
16 treatment by ICSI, 15 (2.6%) presented with congenital abnormalities (9 major and 6 minor abnormalit
17 hild mortality in China, whereas deaths from congenital abnormalities, accidents, and sudden infant d
18 ms, but for 18 countries with reliable data, congenital abnormalities account for a median of only 7.
19 broad categories of death: perinatal causes, congenital abnormalities, acquired natural causes, exter
20 The VCFS phenotype is complex, with multiple congenital abnormalities affecting several tissues and o
21 ith chromosomal fragility, aplastic anaemia, congenital abnormalities and a high risk of cancer, incl
27 st be tightly controlled in order to prevent congenital abnormalities and fetal death which can resul
28 new genetic mechanism that results in human congenital abnormalities and identifies a pathogenetic m
30 hology scores based on the presence of major congenital abnormalities and minor physical anomalies.
31 sorder characterized by bone marrow failure, congenital abnormalities, and an increased risk for canc
32 by progressive bone marrow failure, multiple congenital abnormalities, and an increased risk of cance
33 sorder that can lead to bone marrow failure, congenital abnormalities, and increased risk for leukemi
34 e regulatory elements are capable of causing congenital abnormalities, and possess the capacity to mo
35 characterized by defects in erythropoiesis, congenital abnormalities, and predisposition to cancer.
36 lities, including the presence and extent of congenital abnormalities, aortic disease, intracardiac m
37 is associated with an increased incidence of congenital abnormalities as well as embryonic and perina
38 l disability (ID) and neurological and other congenital abnormalities associated with compound hetero
39 recessive disease characterized by multiple congenital abnormalities, bone marrow failure, and cance
41 is a rare recessive disease characterized by congenital abnormalities, bone marrow failure, and cance
42 a (FA) is a genetic disease characterized by congenital abnormalities, bone marrow failure, and cance
43 (FA) is a genetic disorder characterized by congenital abnormalities, bone marrow failure, and incre
44 (FA) is a genetic disorder characterized by congenital abnormalities, bone marrow failure, and marke
45 a complex genetic disorder characterized by congenital abnormalities, bone marrow failure, and myelo
46 a (FA) is a genetic disease characterized by congenital abnormalities, bone marrow failure, and susce
47 sorder characterized by genomic instability, congenital abnormalities, cancer predisposition and bone
48 sorder characterized by bone marrow failure, congenital abnormalities, cancer susceptibility, and a m
49 M marker concentrations and primary risks of congenital abnormalities, cancer, and Alzheimer disease.
50 erved between rs1801198 and primary risks of congenital abnormalities, cancer, or Alzheimer disease.M
54 a recessive genetic disease characterized by congenital abnormalities, chromosome instability, progre
55 e, the first case report describing multiple congenital abnormalities consistent with MTX embryopathy
56 , the severe mental retardation and multiple congenital abnormalities in a female with a mosaic 45,X/
58 (cryptorchidism) is one of the most frequent congenital abnormalities in humans, involving 2% of male
59 cts in heart development are the most common congenital abnormalities in humans, providing a strong i
60 ence of neural tube defects (NTDs) and other congenital abnormalities in humans, suggesting that foli
65 spread rapidly across Europe and has caused congenital abnormalities in the offspring of cattle, she
69 e and DiGeorge syndrome and lead to multiple congenital abnormalities, including cardiovascular defec
71 of pregnant women can cause a wide range of congenital abnormalities, including microcephaly, in the
72 6,X,t(Y;3)(p11;p12)dn, who exhibits multiple congenital abnormalities, including severe bilateral VUR
74 aths, infants whose mothers died, those with congenital abnormalities, multiple births, and mother an
75 expansion, implicating this mechanism in the congenital abnormalities observed in human infants with
80 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract
81 ariants (8%) in a cohort of individuals with congenital abnormalities of the kidney and urinary tract
82 on C57Bl6 background exhibited a spectrum of congenital abnormalities of the kidney and urinary tract
83 a family with an autosomal dominant form of congenital abnormalities of the kidney or urinary tract
84 ent DSTYK mutations in 2.3% of patients with congenital abnormalities of the kidney or urinary tract,
86 t prevalent in developing countries, whereas congenital abnormalities of the lymphatic system and tra
89 autosomal recessive disease characterized by congenital abnormalities, pancytopenia, and an increased
91 ry and secondary prevention of deaths due to congenital abnormalities, preterm birth complications, a
92 DNA-repair disorder characterized by various congenital abnormalities, progressive bone marrow failur
93 osomal instability syndrome characterized by congenital abnormalities, progressive bone marrow failur
94 FA) is a recessive disorder characterized by congenital abnormalities, progressive bone-marrow failur
95 utosomal recessive condition associated with congenital abnormalities, progressive pancytopenia, and
96 rtality decreased after the neonatal period; congenital abnormalities remained an important cause of
97 he strongest predictor of early BMF in FA; a congenital abnormality score separates patients with nor
99 ginylation knockout mice that lead to severe congenital abnormalities similar to those observed in hu
101 es can alter cellular phenotypes and produce congenital abnormalities such as Down syndrome (DS).
105 the presence or absence of readily diagnosed congenital abnormalities that occur frequently in FA.
106 dy contributes to early pregnancy losses and congenital abnormalities, the causes are unknown and env
107 we analyse the genomes of two patients with congenital abnormalities using the MinION nanopore seque
108 associated with intellectual disability and congenital abnormalities, using array comparative genomi
109 nd medium child mortality countries; whereas congenital abnormalities was the most important cause in
110 nal deficiency, retinal disorders, and other congenital abnormalities were the leading causes of chil
112 miscarriage, stillbirth, pregnancy loss, and congenital abnormality were not statistically different
113 m perinatal causes and there were seven (3%) congenital abnormalities, with no effect of in utero ten
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