infection with lymphocytic choriomeningitis virus in the fetus of a 29-year - old pregnant women at 23 weeks ' gestation.[ncbi.nlm.nih.gov(passive) caused bycongenital microencephaly
usually(passive) is ... causedCongenital hypotonia
Setaria bidentata ( Nematoda : Filarioidea ) in the Red Brocket Deer ( Mazama americana ) 15(passive) Caused byCongenital Filariasis
Setaria bidentata ( Nematoda : Filarioidea ) in the Red Brocket Deer ( Mazama americana ) 14(passive) Caused byCongenital Filariasis
a novel nonsense mutation in the FGB gene in a Palestinian family | Blood Journal Congenital afibrinogenemia(passive) caused bycongenital afibrinogenemia
years intensive glycemic controlpreventscongenital anomalies.]ama
a novel nonsense mutation in the FGB gene in a Palestinian family Neerman Arbez , Marguerite ; Vu , Dung(passive) caused bycongenital afibrinogenemia
a novel nonsense mutation in the FGB gene in a Palestinian family Marguerite Neerman - Arbez , Dung Vu(passive) caused bycongenital afibrinogenemia
Deletion of the fibrinogen alpha - chain gene ( FGAcausescongenital afibrinogenemia
title = " A randomized trial of hyperimmune globulinto preventcongenital cytomegalovirus
2469389112.A randomized trial of hyperimmune globulinto preventcongenital cytomegalovirus
246938913.A randomized trial of hyperimmune globulinto preventcongenital cytomegalovirus
PubMed ] Tirefort , Y. ; Alson , O.R. ; de Moerloose , P. ; Neerman - Arbez , M. Mutation of the translation initiation codon in FGAcausescongenital afibrinogenemia
Study GroupA randomized trial of hyperimmune globulinto preventcongenital cytomegalovirus
Mosca F. A randomized trial of hyperimmune globulinto preventcongenital cytomegalovirus
small molecule diseasescausingcongenital hyperammonemia
recent arterial puncture closing device , collagen hemostatic puncture closure , or fails to improve glycemic controlpreventscongenital anomalies.]ama
125 - 131 71 Tirefort Y , Alson OR , de Moerloose P , Neerman - Arbez M. Mutation of the translation initiation codon in FGAcausescongenital afibrinogenemia
Select item 2469389113.A randomized trial of hyperimmune globulinto preventcongenital cytomegalovirus
LIPH mutations Tanahashi , K. , Sugiura , K. & Akiyama , M.(passive) caused bycongenital hypotrichosis
mutations in the FGA gene other disorders(passive) caused bycongenital afibrinogenemia
a novel nonsense mutation in the FGB gene in a ... | Archive ouverte UNIGE Home Titles list Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a(passive) caused bycongenital afibrinogenemia
a dysfunctional lymphatic vessel formation due to a loss of extracellular response mediated by vascular endothelial growth factor receptor 3 ( VEGFR-3 , MIM 136352(passive) caused bycongenital lymphoedema
a range of genetic disorders or medical conditions(passive) can be caused byCongenital deafblindness
various diseases , including central nervous system disorders , neuromuscular diseases , and genetic disorders(passive) can be caused byCongenital hypotonia
an inherited deficiency in the enzyme NADH - cytochrome b5 reductase , which is responsible for reducing methemoglobin in the blood(passive) is typically caused byCongenital methemoglobinemia
cialis for sale within the facial nerve canaloriginatingcialis for sale within the facial nerve canal
Elizabeth 's birth defects(passive) were caused byElizabeth 's birth defects
hearing loss(passive) caused byhearing loss
82 P - D-3 - 1 - 910 Central Diabetes Insipidus(passive) Caused by82 P - D-3 - 1 - 910 Central Diabetes Insipidus
progressive vision losscausesprogressive vision loss
from abnormal calcium metabolism in epidermal keratinocytesdirectly resultingfrom abnormal calcium metabolism in epidermal keratinocytes
swallow and gag reflux problemscausingswallow and gag reflux problems
from biallelic loss - of - function variants of ERBB3resultingfrom biallelic loss - of - function variants of ERBB3
from abnormal chromosomes and also acquired lymphangioma that are the result of trauma or inflammationresultfrom abnormal chromosomes and also acquired lymphangioma that are the result of trauma or inflammation
to muscle weakness in the hind quarters and less frequently in the front making it difficult for the animal to standleadsto muscle weakness in the hind quarters and less frequently in the front making it difficult for the animal to stand
in early failure to thrive , short stature , global developmental delay , usually mild intellectual disability , genital hypoplasia , hypothalamic hypogonadism , and characteristic behavior problems ( temper tantrums , stubbornness , manipulative behavior , and obsessive - compulsive characteristicsresultingin early failure to thrive , short stature , global developmental delay , usually mild intellectual disability , genital hypoplasia , hypothalamic hypogonadism , and characteristic behavior problems ( temper tantrums , stubbornness , manipulative behavior , and obsessive - compulsive characteristics
from a congenital ( present at birthresultsfrom a congenital ( present at birth
due to a defect in the gene and is not curableis causeddue to a defect in the gene and is not curable
congestive seizures in the newborncausingcongestive seizures in the newborn
in low vision and an abnormal appearance to my right eyeresultedin low vision and an abnormal appearance to my right eye
nasal obstructioncausingnasal obstruction
from an epidermoid formation in the anterior superior lateral tympanic cavity adjacent to the anterior annulus during fetal developmentmay originatefrom an epidermoid formation in the anterior superior lateral tympanic cavity adjacent to the anterior annulus during fetal development
from inherited defectsmay resultfrom inherited defects
them to be born with no haircausesthem to be born with no hair
severe brain damagecausedsevere brain damage
deafness in childrencausingdeafness in children
adjacent to the trigoneoriginateadjacent to the trigone
in abnormal functionresultingin abnormal function
from the same ectoderm which forms a primitive notochord ... and that embryonic cell remnants of this ectodermic structure can occur in any cranial boneoriginatedfrom the same ectoderm which forms a primitive notochord ... and that embryonic cell remnants of this ectodermic structure can occur in any cranial bone
in abnormal functionAcquiredresultingin abnormal functionAcquired
a cat to be born baldcausesa cat to be born bald
to purulent inflammation in the lacrimal sac Dacryocystitis , or partial blockage of the lacrimal canal in childrenleadsto purulent inflammation in the lacrimal sac Dacryocystitis , or partial blockage of the lacrimal canal in children
minor disability in daily lifecausesminor disability in daily life
mental retardation in childrencausesmental retardation in children
generallyoriginatesgenerally
from defective recanalization of duodenal lumen during fetal developmentresultingfrom defective recanalization of duodenal lumen during fetal development