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1 nital heart disease (CHD) is the most common congenital abnormality.
2 of TH perturbation is sufficient to induce a congenital abnormality.
3 ellectual disability and signature brain and congenital abnormalities.
4 ers constitute some of the most common human congenital abnormalities.
5 and management of infants with these common congenital abnormalities.
6 re perinatal outcomes, postnatal health, and congenital abnormalities.
7 12 live births, including three infants with congenital abnormalities.
8 lar proliferation in situ did not reveal any congenital abnormalities.
9 plicated in neurodevelopmental disorders and congenital abnormalities.
10 No babies had congenital abnormalities.
11 currences and are often related to trauma or congenital abnormalities.
12 unosuppressive medication use, or documented congenital abnormalities.
13 44+6 weeks to mothers over 15 years, without congenital abnormalities.
14 the leading genetic cause of miscarriage and congenital abnormalities.
15 previa, gestational diabetes, or a baby with congenital abnormalities.
16 g an unprecedented epidemic linked to severe congenital abnormalities.
17 -threatening infections and subsequent fetal congenital abnormalities.
18 terozygosity (AOH) in subjects with multiple congenital abnormalities.
19 far no definitive link between belimumab and congenital abnormalities.
20 ased approaches to understand the origins of congenital abnormalities.
21 cal deformities caused by trauma, tumors, or congenital abnormalities.
22 Opitz syndrome (SLOS) are born with multiple congenital abnormalities.
23 ue comprehensive views of cardiac valves and congenital abnormalities.
24 arr virus producing lymphoma, carcinoma, and congenital abnormalities.
25 eased risk for giving birth to children with congenital abnormalities.
26 ing causes of under-5 mortality in 2015 were congenital abnormalities (35 700 deaths, 95% uncertainty
27 treatment by ICSI, 15 (2.6%) presented with congenital abnormalities (9 major and 6 minor abnormalit
28 hild mortality in China, whereas deaths from congenital abnormalities, accidents, and sudden infant d
29 ms, but for 18 countries with reliable data, congenital abnormalities account for a median of only 7.
30 broad categories of death: perinatal causes, congenital abnormalities, acquired natural causes, exter
32 The VCFS phenotype is complex, with multiple congenital abnormalities affecting several tissues and o
33 usly identified in individuals with multiple congenital abnormalities affecting the heart, kidney, ve
34 ith chromosomal fragility, aplastic anaemia, congenital abnormalities and a high risk of cancer, incl
35 rder, FA, characterized clinically by severe congenital abnormalities and a very high propensity to d
37 rodent-borne zoonotic arenavirus that causes congenital abnormalities and can be fatal for transplant
44 st be tightly controlled in order to prevent congenital abnormalities and fetal death which can resul
46 d with neurologic complications that include congenital abnormalities and Guillain-Barre syndrome (GB
47 new genetic mechanism that results in human congenital abnormalities and identifies a pathogenetic m
49 hology scores based on the presence of major congenital abnormalities and minor physical anomalies.
50 an cause fetus demise, stillbirth, or severe congenital abnormalities and neurological complications.
51 SI group and 25 in the ICSI group; most were congenital abnormalities and none were attributed to tre
52 ibutions of both rare and common variants to congenital abnormality and adult onset disease are consi
53 sorder characterized by bone marrow failure, congenital abnormalities, and an increased risk for canc
54 by progressive bone marrow failure, multiple congenital abnormalities, and an increased risk of cance
55 sorder that can lead to bone marrow failure, congenital abnormalities, and increased risk for leukemi
56 e regulatory elements are capable of causing congenital abnormalities, and possess the capacity to mo
57 characterized by defects in erythropoiesis, congenital abnormalities, and predisposition to cancer.
58 pregnancy, preterm birth prior to 37 weeks, congenital abnormality, and those undergoing planned ces
59 lities, including the presence and extent of congenital abnormalities, aortic disease, intracardiac m
60 is associated with an increased incidence of congenital abnormalities as well as embryonic and perina
61 l disability (ID) and neurological and other congenital abnormalities associated with compound hetero
62 recessive disease characterized by multiple congenital abnormalities, bone marrow failure, and cance
63 is a rare genetic disorder characterized by congenital abnormalities, bone marrow failure, and cance
65 is a rare recessive disease characterized by congenital abnormalities, bone marrow failure, and cance
66 a (FA) is a genetic disease characterized by congenital abnormalities, bone marrow failure, and cance
67 cer predisposition syndrome characterized by congenital abnormalities, bone marrow failure, and hyper
68 (FA) is a genetic disorder characterized by congenital abnormalities, bone marrow failure, and incre
69 (FA) is a genetic disorder characterized by congenital abnormalities, bone marrow failure, and marke
70 a complex genetic disorder characterized by congenital abnormalities, bone marrow failure, and myelo
71 a (FA) is a genetic disease characterized by congenital abnormalities, bone marrow failure, and susce
72 sorder characterized by genomic instability, congenital abnormalities, cancer predisposition and bone
73 sorder characterized by bone marrow failure, congenital abnormalities, cancer susceptibility, and a m
74 M marker concentrations and primary risks of congenital abnormalities, cancer, and Alzheimer disease.
75 erved between rs1801198 and primary risks of congenital abnormalities, cancer, or Alzheimer disease.M
79 a recessive genetic disease characterized by congenital abnormalities, chromosome instability, progre
80 onset of bone marrow failure and more severe congenital abnormalities compared with a large series of
81 e, the first case report describing multiple congenital abnormalities consistent with MTX embryopathy
82 een implicated in this process and linked to congenital abnormalities, few studies have examined the
83 he cell and is deregulated in human cancers, congenital abnormalities, immune diseases, and neurodeve
84 , the severe mental retardation and multiple congenital abnormalities in a female with a mosaic 45,X/
86 (cryptorchidism) is one of the most frequent congenital abnormalities in humans, involving 2% of male
87 cts in heart development are the most common congenital abnormalities in humans, providing a strong i
88 ence of neural tube defects (NTDs) and other congenital abnormalities in humans, suggesting that foli
95 spread rapidly across Europe and has caused congenital abnormalities in the offspring of cattle, she
98 and to identify what events are disrupted in congenital abnormalities in which muscles fail to form n
100 e and DiGeorge syndrome and lead to multiple congenital abnormalities, including cardiovascular defec
102 ) is a reemerging human pathogen that causes congenital abnormalities, including microcephaly and eye
103 of pregnant women can cause a wide range of congenital abnormalities, including microcephaly, in the
104 6,X,t(Y;3)(p11;p12)dn, who exhibits multiple congenital abnormalities, including severe bilateral VUR
106 aths, infants whose mothers died, those with congenital abnormalities, multiple births, and mother an
107 expansion, implicating this mechanism in the congenital abnormalities observed in human infants with
110 es and is also associated with various other congenital abnormalities of the cardiovascular system.
115 y of kidney disease, extrarenal involvement, congenital abnormalities of the kidney and urinary tract
116 mutations, which have been shown to lead to congenital abnormalities of the kidney and urinary tract
117 ariants (8%) in a cohort of individuals with congenital abnormalities of the kidney and urinary tract
118 on C57Bl6 background exhibited a spectrum of congenital abnormalities of the kidney and urinary tract
119 a family with an autosomal dominant form of congenital abnormalities of the kidney or urinary tract
120 ent DSTYK mutations in 2.3% of patients with congenital abnormalities of the kidney or urinary tract,
122 t prevalent in developing countries, whereas congenital abnormalities of the lymphatic system and tra
124 ete tracheal ring deformity (CTRD) is a rare congenital abnormality of unknown etiology characterized
125 Here, we review the intricacies of these congenital abnormalities, offering an in-depth examinati
127 nsformations are often associated with major congenital abnormalities or pediatric cancers (pleiotrop
128 ogeneous group of disorders characterized by congenital abnormalities or progressive deformation of t
129 death (OR 2.26, CI 1.07 to 4.75, p = 0.032), congenital abnormality (OR 2.71, CI 1.58 to 4.66, p < 0.
130 autosomal recessive disease characterized by congenital abnormalities, pancytopenia, and an increased
133 ry and secondary prevention of deaths due to congenital abnormalities, preterm birth complications, a
134 nia, diarrhoea, meningitis, injury, measles, congenital abnormalities, preterm birth complications, i
135 maternal age of younger than 18 years, major congenital abnormalities, prior participation in this tr
136 osomal instability syndrome characterized by congenital abnormalities, progressive bone marrow failur
137 DNA-repair disorder characterized by various congenital abnormalities, progressive bone marrow failur
138 FA) is a recessive disorder characterized by congenital abnormalities, progressive bone-marrow failur
139 utosomal recessive condition associated with congenital abnormalities, progressive pancytopenia, and
140 rtality decreased after the neonatal period; congenital abnormalities remained an important cause of
141 he strongest predictor of early BMF in FA; a congenital abnormality score separates patients with nor
143 ginylation knockout mice that lead to severe congenital abnormalities similar to those observed in hu
145 es can alter cellular phenotypes and produce congenital abnormalities such as Down syndrome (DS).
148 ine mutations deregulating MEK1 also lead to congenital abnormalities, such as the cardiofaciocutaneo
150 the presence or absence of readily diagnosed congenital abnormalities that occur frequently in FA.
151 dy contributes to early pregnancy losses and congenital abnormalities, the causes are unknown and env
152 we analyse the genomes of two patients with congenital abnormalities using the MinION nanopore seque
153 associated with intellectual disability and congenital abnormalities, using array comparative genomi
154 nd medium child mortality countries; whereas congenital abnormalities was the most important cause in
158 nal deficiency, retinal disorders, and other congenital abnormalities were the leading causes of chil
160 miscarriage, stillbirth, pregnancy loss, and congenital abnormality were not statistically different
161 m perinatal causes and there were seven (3%) congenital abnormalities, with no effect of in utero ten