The spectrum of congenital anomalies of the VATER association: an international study.
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Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?VACTERL/VATER AssociationOesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiologyThe Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approachesThe genetic landscape and clinical implications of vertebral anomalies in VACTERL associationVATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysisEtiology and clinical presentation of birth defects: population based studyVertebral anomalies in a new family with ODED syndrome.VATER non-random association of congenital malformations: study based on data from four malformation registers.Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.Childhood cancer risk in those with chromosomal and non-chromosomal congenital anomalies in Washington State: 1984-2013The VACTERL association: lessons from the Sonic hedgehog pathway.Inheritance of the VATER/VACTERL association.Consideration of VACTERL association in patients with trisomy 21.Modern imaging of the tracheo-bronchial tree.Analysis of renal anomalies in VACTERL association.Long-term outcomes of adults with features of VACTERL association.Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL associationEphrin-B reverse signaling controls septation events at the embryonic midline through separate tyrosine phosphorylation-independent signaling avenuesAnalysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association.Growth failure and pituitary function in CHARGE and VATER associations.Kidney transplantation in an adult patient with VACTERL associationSirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review.Challenges in Studying Modifiable Risk Factors for Birth DefectsVertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literatureVATER/VACTERL Association: Evidence for the Role of Genetic FactorsMitochondrial Factors and VACTERL Association-Related Congenital MalformationsAdriamycin-Induced Models of VACTERL Association.VACTERL-H Association and Fanconi Anemia.Considering the Embryopathogenesis of VACTERL AssociationAnorectal malformations associated with esophageal atresia in neonates.De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.Familial occurrence of the VATER/VACTERL association.Persistent right aortic arch and associated axial skeletal malformations in cats.Associations of anorectal malformations and related syndromes.VACTERL association with double-chambered left ventricle: A rare occurrence.First Trimester Diagnosis of VACTERL Association.Genetic Syndromes Affecting Kidney Development.Mullerian dysgenesis: a critical review of the literature.
P2860
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P2860
The spectrum of congenital anomalies of the VATER association: an international study.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
The spectrum of congenital anomalies of the VATER association: an international study.
@en
The spectrum of congenital anomalies of the VATER association: an international study.
@nl
type
label
The spectrum of congenital anomalies of the VATER association: an international study.
@en
The spectrum of congenital anomalies of the VATER association: an international study.
@nl
prefLabel
The spectrum of congenital anomalies of the VATER association: an international study.
@en
The spectrum of congenital anomalies of the VATER association: an international study.
@nl
P2093
P2860
P50
P1476
The spectrum of congenital anomalies of the VATER association: an international study.
@en
P2093
Castilla EE
Czeizel AE
Lancaster PA
Martínez-Frías ML
Mastroiacovo P
P2860
P356
10.1002/(SICI)1096-8628(19970711)71:1<8::AID-AJMG2>3.0.CO;2-V
P577
1997-07-01T00:00:00Z