About: Extending the scope of the VATER association: definition of the VATER syndrome

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About: Extending the scope of the VATER association: definition of the VATER syndrome Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1974 (uk) im September 1974 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57930518-43681698-A60D-4300-AE4C-19BE374F43B8
publication date	1974-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57930518-579D9340-2E9C-4C77-9644-B5CBFA192723
language of work or name	English
cites work	wds:Q57930518-0488548A-E639-46F1-8A3C-7BC8EEF9642C wds:Q57930518-190E6BE4-3007-466B-A440-6701D787EEBC wds:Q57930518-2DE51AD9-63C8-4645-8542-E43017CAC575 wds:Q57930518-4F654183-91C4-462C-AD71-9CB080A5ED46 wds:Q57930518-57B4E817-6A9A-472A-AA2C-564E6412FDEB wds:Q57930518-68FBB9CB-1F5A-4215-A133-4F3C34DCE3B0 wds:Q57930518-9CEF0427-C94E-48AC-AB57-0AF6DB857694 wds:Q57930518-A2AD2675-D4EF-42D2-BD43-A4E9A97E03C5 wds:Q57930518-A407EE27-9642-4050-BAA0-21A3DF614BA2 wds:Q57930518-A69666B3-5FD0-413F-BDFB-B400A4033B78 wds:Q57930518-B0E6F207-D5E3-4AFD-ACF4-B9E4F57631E8 wds:Q57930518-B7950E74-8E0A-45AA-BE50-620D5C1050C7 wds:Q57930518-CDEF5CD2-4A3D-4CD0-9B97-F167429C46AF wds:Q57930518-DE380FD8-F1C7-4A46-8787-3245AEBA0443 wds:Q57930518-E955989C-670D-4192-8F7D-FFE5B8B938E0 wds:Q57930518-ECE89393-211D-4250-8FDC-13A8D6F90221
cites work	Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies A COMPLEX OF ANOMALIES ASSOCIATED WITH TRACHEOESOPHAGEAL FISTULA AND ESOPHAGEAL ATRESIA The VATER association. Vertebral defects, Anal atresia, T-E fistula with esophageal atresia, Radial and Renal dysplasia: a spectrum of associated defects A new polydactyly/imperforate-anus/vertebral-anomalies syndrome? Congenital malformation of the heart associated with congenital anomalies of the urinary tract, including a syndrome of ventricular septal defect, pulmonary hypertension, mental retardation, and skeletal deformity. Genesis of single umbilical artery Extra vertebrae associated with esophageal atresias and tracheoesophageal fistulas Birth defects and oral contraceptives A new syndrome of dysmorphogenesis: imperforate-anus associated with poly-oligodactyly and skeletal (mainly vertebral) anomalies Absent Umbilical Artery: A Review of 113 Cases Imperforate anus/polydactyly/vertebral anomalies syndrome: A hereditary trait? The polydactyly--imperforate-anus--vertebral-anomalies syndrome. A new polydactyly-imperforate-anus-vertebral-anomalies syndrome? Polydactyly/imperforate-anus/vertebral-anomalies syndrome A new polydactyly/imperforate-anus/vertebral-anomalies syndrome Anomalies associated with congenital deformities of the thumb
author name string	wds:Q57930518-3BCB501F-09F4-42CA-A12E-E00789468E29 wds:Q57930518-47A7F770-AA56-47FD-BF7D-87D60786E011 wds:Q57930518-4EED6CA7-12F7-42C8-BB6D-63F24A1554F6 wds:Q57930518-69FE37C4-50ED-4E65-BAEC-65088E327623
author name string	J D Miller S A Temtamy Samia A. Temtamy J. Daniel Miller
rdfs:label	Extending the scope of the VATER association: definition of the VATER syndrome (en) Extending the scope of the VATER association: definition of the VATER syndrome (nl)
skos:prefLabel	Extending the scope of the VATER association: definition of the VATER syndrome (en) Extending the scope of the VATER association: definition of the VATER syndrome (nl)
name	Extending the scope of the VATER association: definition of the VATER syndrome (en) Extending the scope of the VATER association: definition of the VATER syndrome (nl)
title	wds:Q57930518-6B1912DF-4FE7-4DE5-9E2C-994DC8F3011E wds:Q57930518-EF34704C-E4DD-41EE-80A7-7D6593D622FC
title	Extending the scope of the VATER association: definition of the VATER syndrome (en) Extending the scope of the VATER association: Definition of the VATER syndrome (en)
page(s)	wds:Q57930518-3021E219-CF44-491C-A90A-CBD3611CAEA3 wds:Q57930518-4E0858C9-7DCB-41F2-A9BD-2199728A36F1
page(s)	345-349 345-9
instance of	wds:Q57930518-981B3047-70F0-4D27-95E5-4B33E3A7AE3D
instance of	scholarly article
main subject	wds:Q57930518-B0DD067F-983B-4291-AC42-7805C64A4CB2 wds:Q57930518-F27BA155-9BAA-42FF-B86E-45EC84F86915
main subject	Vater VATER syndrome
PubMed ID	wds:Q57930518-744BC7B4-317F-4E5E-A1FD-7850A6E059D5
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4372554
PubMed ID	4372554
published in	wds:Q57930518-302055F8-F3E5-419E-89B6-B3D9DCF2D107
published in	The Journal of Pediatrics
issue	wds:Q57930518-EF5930B6-82D0-454A-8509-C9A1DC766999
volume	wds:Q57930518-06961F02-9860-4734-85F6-1692A1B26314
issue	3
volume	85
DOI	wds:Q57930518-431CD758-D2F9-4DD5-B80F-A66CFAF2D3E2
DOI	http://dx.doi.org/10.1016/S0022-3476(74)80113-7
DOI	10.1016/S0022-3476(74)80113-7
skos:altLabel	Extending the scope of the VATER association: Definition of the VATER syndrome (en) Extending the scope of the VATER association: Definition of the VATER syndrome (nl)
is owl:sameAs of	Extending the scope of the VATER association: definition of the VATER syndrome
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57930518
is cites work of	VACTERL anomalies in patients with esophageal atresia: an updated delineation of the spectrum and review of the literature The Vater association: malformations of the male external genitalia High proximal pouch esophageal atresia with vertebral, rib, and sternal anomalies: An additional component to the VATER association The VACTERL association: lessons from the Sonic hedgehog pathway The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches Autosomal dominant transmission of a syndrome of anal, ear, renal, and radial congenital malformations Ephrin-B reverse signaling controls septation events at the embryonic midline through separate tyrosine phosphorylation-independent signaling avenues A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus Congenital corneal anaesthesia and the MURCS association: a case report The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia Etiological heterogeneity in sirenomelia Interrelationships of the hemifacial microsomia-VATER, VATER, and sirenomelia phenotypes Holt-Oram syndrome Ocular findings in CHARGE syndrome. Six case reports and a review Malformations associated with congenital absence of the gall bladder

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