Literature DB >> 6352947

Does sacral agenesis predispose to spina bifida?

R Magnus, J G Rogers, E A Haan.   

Abstract

Mesh：

Year:  1983        PMID： 6352947      PMCID： PMC1049129          DOI： 10.1136/jmg.20.4.313

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  12 in total

1.  Sacral agenesis. Analysis of 22 cases.

Authors:  R I White; G T Klauber
Journal:  Urology       Date:  1976-12       Impact factor: 2.649

2.  [Familial sacro-coccygeal agenesis. Apropos of 6 cases in 2 families].

Authors:  J Robert; J Pernod; R Bonnet
Journal:  J Genet Hum       Date:  1974-03

3.  Occult spinal dysraphism: a series of 73 cases.

Authors:  F M Anderson
Journal:  Pediatrics       Date:  1975-06       Impact factor: 7.124

4.  Sacral agenesis: an analysis of 11 cases and review of the literature.

Authors:  A J Mariani; J Stern; A U Khan; A S Cass
Journal:  J Urol       Date:  1979-11       Impact factor: 7.450

5.  Chondromalacia Patellae. A prospective study.

Authors:  J Insall; K A Falvo; D W Wise
Journal:  J Bone Joint Surg Am       Date:  1976-01       Impact factor: 5.284

6.  Sacral agenesis: a clinical evaluation of its management, heredity, and associated anomalies.

Authors:  J Andrish; A Kalamchi; G D MacEwen
Journal:  Clin Orthop Relat Res       Date:  1979 Mar-Apr       Impact factor: 4.176

7.  Sacral agenesis with progressive neurological deficit.

Authors:  D Pang; H J Hoffman
Journal:  Neurosurgery       Date:  1980-08       Impact factor: 4.654

8.  Familial caudal regression anomalad and maternal diabetes.

Authors:  J M Stewart; S Stoll
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

9.  Congenital sacral anomalies.

Authors:  J K Stanley; R Owen; S Koff
Journal:  J Bone Joint Surg Br       Date:  1979-11

10.  A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.

Authors:  M Fellous; J Boué; C Malbrunot; E Wollman; M Sasportes; N Van Cong; A Marcelli; R Rebourcet; C Hubert; F Demenais; R C Elston; K K Namboodiri; E B Kaplan; M Fellous
Journal:  Am J Med Genet       Date:  1982-08
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