Literature DB >> 5345108

Chromosome abnormalities in two cases with bilateral radial element defects.

M Faed, A Stewart, A J Keay.   

Abstract

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Mesh：

Year:  1969        PMID： 5345108      PMCID： PMC1468742          DOI： 10.1136/jmg.6.3.342

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


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  11 in total

1.  PHOCOMELIA AND TRISOMY E.

Authors:  H ZELLWEGER; D S HUFF; G ABBO
Journal:  Acta Genet Med Gemellol (Roma)       Date:  1965-04

2.  PALM-PRINTS AND A RING-D CHROMOSOME.

Authors:  M S ADAMS
Journal:  Lancet       Date:  1965-09-04       Impact factor: 79.321

3.  [Partial trisomy 18 caused by insertion or translocation 4/18].

Authors:  F GAGNON; L ARCHAMBAULT; E LABERGE; N KATYK-LONGTIN
Journal:  Union Med Can       Date:  1963-03

4.  Multiple congenital abnormalities associated with ring chromosome.

Authors:  A D BAIN; I K GAULD
Journal:  Lancet       Date:  1963-08-10       Impact factor: 79.321

5.  Chronic pancytopenia with multiple congenital abnormalities (Fanconi's anaemia).

Authors:  L R NILSSON
Journal:  Acta Paediatr       Date:  1960-07       Impact factor: 2.299

6.  A new human trisomy?

Authors:  M Gonzalez-Ramos; M A Ahedo
Journal:  Lancet       Date:  1968-09-21       Impact factor: 79.321

7.  "Cri du Chat" due to a ring-B chromosome.

Authors:  R A Rohde; R Tompkins
Journal:  Lancet       Date:  1965-11-20       Impact factor: 79.321

8.  Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues.

Authors:  M R Swift; K Hirschhorn
Journal:  Ann Intern Med       Date:  1966-09       Impact factor: 25.391

9.  [Spontaneous chromosome aberrations in familial panmyelopathy].

Authors:  T M Schroeder; F Anschütz; A Knopp
Journal:  Humangenetik       Date:  1964

10.  Absent thumbs with a ring D2 chromosome: a new deletion syndrome.

Authors:  R S Sparkes; R E Carrel; S W Wright
Journal:  Am J Hum Genet       Date:  1967-09       Impact factor: 11.025
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  11 in total

1.  Derivative chromosomal structures from a ring chromsome 4.

Authors:  R Niss; E Passarge
Journal:  Humangenetik       Date:  1975-05-26

2.  A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype.

Authors:  A Carnevale; L De los Cobos
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

3.  Deletion from the long arm of chromosome 4 (46,XX,4q-) associated with congenital anomalies.

Authors:  M S Golbus; F A Conte; D L Daentl
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

4.  Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease.

Authors:  M Faed; H G Morton; J Robertson
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

5.  Congenital heart disease in radial clubbed hand syndrome.

Authors:  A Simcha
Journal:  Arch Dis Child       Date:  1971-06       Impact factor: 3.791

6.  A complex chromosomal rearrangement with formation of a ring 4.

Authors:  M Bobrow; L F Joness; G Clarke
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

7.  The 13q- deletion syndrome.

Authors:  E Grace; J Drennan; D Colver; R R Gordon
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

8.  A ring-4 chromosome in a patient with normal intelligence and short stature.

Authors:  R B Surana; J D Bailey; P E Conen
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

9.  Child with multiple anomalies and a group B(4-5) long arm deletion (Bq-).

Authors:  R H Lindenbaum; L J Butler
Journal:  Arch Dis Child       Date:  1971-02       Impact factor: 3.791

10.  Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm.

Authors:  R Bernstein; A T Milne; T Jenkins
Journal:  J Med Genet       Date:  1978-08       Impact factor: 6.318
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