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1  formation are the most common serious human congenital defect.
2 ation with increased risk of miscarriage and congenital defects.
3  gene haploinsufficiency causes a variety of congenital defects.
4  light on the developmental underpinnings of congenital defects.
5 ysis in developmental pathologies, including congenital defects.
6 ut not other pathogenic flaviviruses, causes congenital defects.
7 occurs, can lead to abnormal development and congenital defects.
8 ure of which results in clinically important congenital defects.
9 sive surgery and in heart surgery to correct congenital defects.
10 improved survivals for even the most complex congenital defects.
11 s the DAG-PKC cascade and is correlated with congenital defects.
12 a leading cause of frequent miscarriages and congenital defects.
13 fects and control infants (n = 3,029) had no congenital defects.
14 s as a result of trauma, tumor resection, or congenital defects.
15 n (3), aspiration (6), panbronchiolitis (1), congenital defect (1), ABPA (11), rheumatoid arthritis (
16  tetraplegia, 81% learning difficulties, 60% congenital defects, 41% neuropsychiatric problems and 28
17  Cardiomelic or heart-hand syndromes include congenital defects affecting both the forelimb and heart
18 edgehog (Hh) signaling is implicated in both congenital defects and cancers arising from the gastroin
19           These AP-2-null mice have multiple congenital defects and die at birth.
20                                    Surges in congenital defects and Guillain-Barre syndrome alerted t
21 can occur as a result of injury, disease, or congenital defects and treatment options are often limit
22 ses, matched to living controls by age, sex, congenital defect, and surgical repair.
23 sitivity to DNA damage, bone marrow failure, congenital defects, and cancer.
24 ling has been implicated in various cancers, congenital defects, and cardiovascular diseases.
25         Trauma, cancer, birth complications, congenital defects, and other surgical diseases potentia
26 cessively inherited disease characterized by congenital defects, bone marrow failure and cancer susce
27  is an autosomal recessive disease marked by congenital defects, bone marrow failure, and cancer susc
28 a (FA) is a genetic disease characterized by congenital defects, bone marrow failure, and cancer susc
29  is an autosomal recessive disease marked by congenital defects, bone marrow failure, and high incide
30 ies account for about one-third of all human congenital defects, but our understanding of the genetic
31 ous potential for bone reconstructions after congenital defects, cancer resections, and trauma.
32     The patient groups with the most complex congenital defects carried the greatest risk of AF and c
33 ren with intellectual disability and various congenital defects (cases) to CNVs in 8,329 unaffected a
34  signaling may contribute to pathogenesis of congenital defects caused by PKP2 deficiency.
35               Opitz G/BBB syndrome (OS) is a congenital defect characterized by hypertelorism and hyp
36 ion in humans causes primary microcephaly, a congenital defect characterized by severe reductions in
37 logies, including developmental abnormality, congenital defect, chronic otitis media with cholesteato
38                                     Although congenital defects impairing this peristalsis are a lead
39  by studying helper T cells from mice with a congenital defect in CD4 expression.
40      Clefting of the soft palate occurs as a congenital defect in humans and adversely affects the ph
41 ce of PLN HEVs in plt/plt mice, which have a congenital defect in T cell homing to PLNs.
42         Hyperinsulinism of infancy (HI) is a congenital defect in the regulated release of insulin fr
43 eatable form of male infertility caused by a congenital defect in the secretion or action of gonadotr
44 indings are relevant to our understanding of congenital defects in cardiac chamber morphogenesis.
45               Analyses of mouse strains with congenital defects in different aspects of secondary lym
46 ial for understanding respiratory disorders, congenital defects in human neonates, and how the disrup
47  that the susceptibility of this junction to congenital defects in humans, such as ureteral-pelvic ob
48               Heart malformations are common congenital defects in humans.
49 ious disease among the immunocompromised and congenital defects in newborns, human cytomegalovirus (H
50 nd/or fetal spontaneous abortion, death, and congenital defects in pregnant women treated with any of
51 olt-Oram syndrome, which is characterized by congenital defects in the heart and upper extremities.
52                                              Congenital defects in the Na/H exchanger regulatory fact
53 ildhood cancers, and a complex assortment of congenital defects including skeletal abnormalities.
54 s offer promise for traumatic bone injuries, congenital defects, non-union fractures and other skelet
55    Patched expression is compatible with the congenital defects observed in the nevoid basal cell car
56  occurred in 31 (1.7%) versus 33 (1.8%), and congenital defects occurred in 18 (1.0%) versus 20 (1.1%
57                                    The first congenital defect of hypoxia-sensing homozygosity for VH
58                             Hypospadias is a congenital defect of the external genitalia that results
59 okitansky-Kuster-Hauser (MRKH) syndrome is a congenital defect of the Mullerian ducts characterized b
60  Vein of Galen malformations (VGMs) are rare congenital defects of cerebral vessels.
61 in vitamin deficiency states and in cases of congenital defects of one-carbon metabolism.
62                                 The exocrine congenital defects of Prox1(DeltaPanc) pancreata appeare
63 ected by craniofacial deformations caused by congenital defects or trauma.
64 ed rate of 11.3 for the Metropolitan Atlanta Congenital Defects Program counties (p = 0.052), both of
65 cords obtained from the Metropolitan Atlanta Congenital Defects Program, which conducts active, popul
66 try modification of the Metropolitan Atlanta Congenital Defects Program.
67 emia (FA) is a rare disease characterized by congenital defects, progressive bone marrow failure and
68 e novel insights into the etiology of common congenital defects such as cleft palate.
69 rate eye and improper development results in congenital defects, such as microphthalmia or anophthalm
70 r (AV) electrical conduction can result from congenital defects, surgical interventions, and maternal
71 TnT4 was significantly higher in hearts with congenital defects that caused congestive failure than i
72                         Traumatic wounds and congenital defects that require large-scale bone tissue
73 Thus, ES cells have the potential to reverse congenital defects through Id-dependent local and long-r
74                                              Congenital defects, trauma, and disease can compromise t
75                                     Multiple congenital defects were observed in the CNS of PDGF-C-nu
76      Partial absence of the sacrum is a rare congenital defect which also occurs as an autosomal domi

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