Literature DB >> 14101502

A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME.

J L HAMERTON, F GIANNELLI, C O CARTER.   

Abstract

Keywords:  BLOOD CHEMICAL ANALYSIS; BLOOD GROUPS; CHOLINESTERASE; CHROMOSOMES; DERMATOGLYPHICS; HAPTOGLOBINS; HEMOGLOBIN; MONGOLISM; TRANSFERRIN

Mesh：

Substances：

Year:  1963        PMID： 14101502     DOI： 10.1159/000129779

Source DB:  PubMed          Journal:  Cytogenetics        ISSN： 0011-4537


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  12 in total

1.  Familial balanced translocation 4p+/17q- as a suggested cause of primary trisomy-21 Down's syndrome.

Authors:  K Oikawa; M Trent; R Lebovitz
Journal:  Arch Dis Child       Date:  1977-11       Impact factor: 3.791

2.  Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

Authors:  I A Uchida; V C Freeman
Journal:  Hum Genet       Date:  1986-02       Impact factor: 4.132

3.  Diverse chromosomal anomalies in a family.

Authors:  L Atkins; C S Bartsocas; P J Porter
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

4.  A t(13q14q) family with the translocation and a Philadelphia chromosome in one member.

Authors:  J Wennström; J Schröder
Journal:  Humangenetik       Date:  1973

Review 5.  Down's syndrome. Current stage of cytogenetic research.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

6.  Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p).

Authors:  C G Palmer; P M Conneally; J C Christian
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

7.  Double chromosomal aberration. Trisomy G and the balanced translocation t(3p--;17q+).

Authors:  I Subrt; H Prchliková
Journal:  Humangenetik       Date:  1969-10

8.  A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.

Authors:  R H Lindenbaum; N L Blackwell; D J De Sa'
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

9.  A family with D-D translocation.

Authors:  E Krmpotic; K Ramanathan; A Grossman
Journal:  J Med Genet       Date:  1968-09       Impact factor: 6.318

10.  A case of Turner's syndrome with familial balanced translocation t(1;2)(q32;q21)mat.

Authors:  I Kondo; H Hamaguchi; A Matsuura; H Nakajima; A Koyama; H Takita
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318
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