Literature DB >> 4379334

Familial 2/3 translocation.

R L Summitt.   

Abstract

Mesh：

Year:  1966        PMID： 4379334      PMCID： PMC1706162     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  20 in total

1.  PARTIAL TRISOMY-DEFICIENCY SYNDROME RESULTING FROM A RECIPROCAL TRANSLOCATION IN A LARGE KINDRED.

Authors:  I A UCHIDA; H C WANG; O E LAXDAL; W A ZALESKI; B P DUNCAN
Journal:  Cytogenetics       Date:  1964

2.  [FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"].

Authors:  J LEJEUNE; J LAFOURCADE; R BERGER; R TURPIN
Journal:  C R Hebd Seances Acad Sci       Date:  1964-06-08

3.  [FAMILIAL 2 - 22 TRANSLOCATION; ASSOCIATION WITH A HAPLO-X TURNER'S SYNDROME].

Authors:  J LEJEUNE; J LAFOURCADE; C SALMON; R TURPIN
Journal:  Ann Genet       Date:  1963

4.  A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.

Authors:  K H GUSTAVSON; S C FINLEY; W H FINLEY; B JALLING
Journal:  Acta Paediatr       Date:  1964-03       Impact factor: 2.299

5.  PRESUMED TRANSLOCATION OF CHROMOSOME NUMBER 2 AND ONE OF THE D GROUP.

Authors:  R D MERCER; G DARAKJIAN
Journal:  Cleve Clin Q       Date:  1963-10

6.  Familial translocation mongolism: a carrier exhibiting nonacrocentric translocation.

Authors:  K BECKER; A ALBERT
Journal:  Proc Staff Meet Mayo Clin       Date:  1963-06-19

7.  Dermal patterns of 18 and D1 trisomics.

Authors:  I A UCHIDA; K PATAU; D W SMITH
Journal:  Am J Hum Genet       Date:  1962-12       Impact factor: 11.025

8.  Normal arotype/translocation mosaic.

Authors:  W SCHMID; D HATFIELD
Journal:  Cytogenetics       Date:  1962

9.  Chromosomal translocations in patients with mongolism and in their normal relatives.

Authors:  W R BREG; O J MILLER; R D SCHMICKEL
Journal:  N Engl J Med       Date:  1962-04-26       Impact factor: 91.245

10.  Chromosome translocation as a cause of familial mongolism.

Authors:  C O CARTER; J L HAMERTON; P E POLANI; A GUNALP; S D WELLER
Journal:  Lancet       Date:  1960-09-24       Impact factor: 79.321
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  6 in total

1.  Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.

Authors:  R L Summitt; A T Tharapel; R S Wilroy
Journal:  Eur J Pediatr       Date:  1977-07-01       Impact factor: 3.183

2.  A cytogenetic survey of 200 unclassifiable mentally retarded children with congenital anomalies and 200 normal controls.

Authors:  A T Tharapel; R L Summitt
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

3.  [Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+].

Authors:  K Bender; H Reinwein; L Z Gorman; U Wolf
Journal:  Humangenetik       Date:  1969-10

4.  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

5.  New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q.

Authors:  S Stengel-Rutkowski; J D Murken; V Pilar; B Dutrillaux; A Rodewald; R Goebel; R Bassermann
Journal:  Eur J Pediatr       Date:  1979-02-08       Impact factor: 3.183

6.  Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

Authors:  P W Allderdice; N Browne; D P Murphy
Journal:  Am J Hum Genet       Date:  1975-11       Impact factor: 11.025
  6 in total

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