Literature DB >> 5345105

Multiple congenital anomalies associated with a ring-D chromosome.

R C Juberg, M S Adams, W J Venema, M G Hart.   

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Year:  1969        PMID： 5345105      PMCID： PMC1468734          DOI： 10.1136/jmg.6.3.314

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


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  28 in total

1.  X-ray-induced chromosome damage in man.

Authors:  I M TOUGH; K E BUCKTON; A G BAIKIE; W M COURT-BROWN
Journal:  Lancet       Date:  1960-10-15       Impact factor: 79.321

2.  Chromosome anomalies.

Authors:  F Hecht; R G Weleber; E R Giblett
Journal:  Lancet       Date:  1967-04-15       Impact factor: 79.321

3.  A ring X chromosome in dwarfism.

Authors:  A D Bain; I K Gauld; J W Farquhar
Journal:  Lancet       Date:  1965-04-10       Impact factor: 79.321

4.  "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

5.  The "D" (13-15) trisomy syndrome: an analysis of 7 examples.

Authors:  G J Snodgrass; L J Butler; N E France; L Crome; A Russell
Journal:  Arch Dis Child       Date:  1966-06       Impact factor: 3.791

6.  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

7.  A ring D chromosome and anomalous inheritance of haptoglobin type.

Authors:  P S Gerald; S Warner; J D Singer; P A Corcoran; I Umansky
Journal:  J Pediatr       Date:  1967-02       Impact factor: 4.406

8.  An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development.

Authors:  L Atkins; R T Sceery; M E Keenan
Journal:  J Med Genet       Date:  1966-06       Impact factor: 6.318

9.  An XO-X ring X chromosome mosaicism in an individual with normal secondary sexual development.

Authors:  A M Bishop; C E Blank; K Simpson; C J Dewhurst
Journal:  J Med Genet       Date:  1966-06       Impact factor: 6.318

10.  Chromosome analysis of solid tumors. I. Twenty-eight nonepithelial tumors.

Authors:  C P Miles
Journal:  Cancer       Date:  1967-08       Impact factor: 6.860
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  9 in total

Review 1.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

Review 2.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

3.  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

4.  The syndrome associated with the partial D-monosomy. Case report and review.

Authors:  D J Orbeli; I W Lurie; J L Goroshenko
Journal:  Humangenetik       Date:  1971

5.  Human chromosomal deficiency: the 4p--syndrome.

Authors:  E Passarge; H C Altrogge; R A Rüdiger
Journal:  Humangenetik       Date:  1970-08-17

6.  Dq-, Dr and retinoblastoma.

Authors:  A I Taylor
Journal:  Humangenetik       Date:  1970

7.  On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.

Authors:  K Bender; K Burckhardt
Journal:  Humangenetik       Date:  1970

8.  [Observation of the 13-15 chromosome group in a ring (46,XY,15r)].

Authors:  J M Emberger; D Rossi; R Jean; H Bonnet; R Dumas
Journal:  Humangenetik       Date:  1971

9.  Radiographic findings in 13q-syndrome.

Authors:  S C Kaste; C B Pratt
Journal:  Pediatr Radiol       Date:  1993
  9 in total

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