Literature DB >> 6074386

[Defects of the femur and fibula with amelia, peromelia or ulnar defects of the arm. A syndrome].

D Kühne, W Lenz, D Petersen, H Schönenberg.   

Abstract

Entities:  

Mesh：

Year:  1967        PMID： 6074386     DOI： 10.1007/bf00273126

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  15 in total

1.  CONGENITAL ABSENCE OF THE FIBULA.

Authors:  M SULAMAA; S RYOEPPY
Journal:  Acta Orthop Scand       Date:  1963

2.  [MALFORMATION OF THE LEGS AND CAUDAL SECTION OF THE SPINE IN INFANTS BORN TO DIABETIC MOTHERS].

Authors:  J KUCERA; W LENZ; W MAIER
Journal:  Dtsch Med Wochenschr       Date:  1965-05-14       Impact factor: 0.628

3.  Thalidomide embryopathy.

Authors:  H SCHONENBERG
Journal:  Ann Paediatr       Date:  1963

4.  [On the currently frequent reduction on deformities of the extremities].

Authors:  H SCHOENENBERG
Journal:  Monatsschr Kinderheilkd       Date:  1962-12

5.  [The incidence of congenital abnormalities of the upper extremities in the Federal Republic of Germany].

Authors:  O HEPP
Journal:  Med Klin       Date:  1962-03-16

6.  Congenital absence of the fibula.

Authors:  A W FARMER; C A LAURIN
Journal:  J Bone Joint Surg Am       Date:  1960-01       Impact factor: 5.284

7.  [Anomalies of the skeleton as radiation injury?].

Authors:  J KOLAR
Journal:  Fortschr Geb Rontgenstr Nuklearmed       Date:  1962-02

8.  [Abnormalities in undesired children].

Authors:  H UHLIG
Journal:  Arztl Wochensch       Date:  1957-01-18

9.  [Deformed extremities in uterus bicornis bicollis].

Authors:  E KRAUSSOLD
Journal:  Z Geburtshilfe Gynakol       Date:  1954

10.  [Thalidomide embryopathy].

Authors:  W LENZ; K KNAPP
Journal:  Dtsch Med Wochenschr       Date:  1962-06-15       Impact factor: 0.628
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  6 in total

1.  Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.

Authors:  S A Al-Awadi; A S Teebi; T I Farag; K M Naguib; M Y el-Khalifa
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

2.  Poly-, syn- and oligodactylyl, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs--a new autosomal recessive syndrome.

Authors:  W Fuhrmann; A Fuhrmann-Rieger; F de Sousa
Journal:  Eur J Pediatr       Date:  1980-03       Impact factor: 3.183

Review 3.  Limb/pelvis-hypoplasia/aplasia syndrome (Al-Awadi/Raas-Rothschild syndrome): report of two Italian sibs and further confirmation of autosomal recessive inheritance.

Authors:  G Camera; G Ferraiolo; D Leo; A Spaziale; S Pozzolo
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

Review 4.  The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review.

Authors:  T I Farag; S A al-Awadi; M J Marafie; L Bastaki; S A al-Othman; F M Mohammed; I S AlSuliman; D S Murthy
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

5.  Familial occurrence of severe ulnar aplasia and lobster claw feet: a new syndrome.

Authors:  H van den Berghe; J Dequeker; J P Fryns; G David
Journal:  Hum Genet       Date:  1978-05-16       Impact factor: 4.132

6.  FFU complex: an analysis of 491 cases.

Authors:  W Lenz; M Zygulska; J Horst
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132
  6 in total

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