Literature DB >> 5927877

Familial reciprocal C/18 translocation.

H H Punnet, L Pinsky, A M Digeorge, R J Gorlin.   

Abstract

Mesh：

Year:  1966        PMID： 5927877      PMCID： PMC1706204     

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


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  15 in total

1.  [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

Authors:  J DE GROUCHY; P ROYER; C SALMON; M LAMY
Journal:  Pathol Biol       Date:  1964-05

2.  A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS.

Authors:  M LUCAS; N H KEMP; J R ELLIS; R MARSHALL
Journal:  Ann Hum Genet       Date:  1963-11       Impact factor: 1.670

3.  MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.

Authors:  J LINDSTEN; M FRACCARO; H P KLINGER; P ZETTERQVIST
Journal:  Cytogenetics       Date:  1965

4.  [CRANIOMETAPHYSIAL DYSPLASIA (PYLE)].

Authors:  J SPRANGER; K PAULSEN; W LEHMANN
Journal:  Z Kinderheilkd       Date:  1965-06-02

5.  Ring chromosomes in human beings.

Authors:  H C WANG; J MELNYK; L T McDONALD; I A UCHIDA; D H CARR; B GOLDBERG
Journal:  Nature       Date:  1962-08-18       Impact factor: 49.962

6.  A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Authors:  P J WAARDENBURG
Journal:  Am J Hum Genet       Date:  1951-09       Impact factor: 11.025

7.  Delayed ontogenesis in human trisomy syndromes.

Authors:  B Hall
Journal:  Hereditas       Date:  1965       Impact factor: 3.271

8.  [6-12 13-15 translocation and partial 6-12 trisomy (probably 10)].

Authors:  J de Grouchy; J Canet
Journal:  Ann Genet       Date:  1965

9.  [On two familial cases of complex translocations].

Authors:  J Lejeune; R Burger
Journal:  Ann Genet       Date:  1965

10.  A family with balanced D1-Cs-translocation carriers and unbalanced offspring.

Authors:  G R Stalder; E M Buhler; G Gadola; R Widmer; F Freuler
Journal:  Humangenetik       Date:  1964
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  7 in total

1.  Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.

Authors:  A J Ebbin; M G Wilson; J W Towner; J P Slaughter
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

2.  [De novo translocation of C-E in clinically atypical E-trisomy syndrome-mosaic: 46,X XX-46, XX, E+, C-t (Cq-; Ep+)].

Authors:  J Hansen
Journal:  Klin Wochenschr       Date:  1970-10-01

3.  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

4.  A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.

Authors:  M J Thornburn; E H Smith-Read; J E Peck
Journal:  Arch Dis Child       Date:  1969-02       Impact factor: 3.791

5.  Familial transmission of a chromosomal translocation t(2q+;Cp-).

Authors:  C B Lozzio; A A Kattine
Journal:  J Med Genet       Date:  1969-06       Impact factor: 6.318

6.  [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].

Authors:  C Laurent; M Bovier-Lapierre; B Dutrillaux
Journal:  Humangenetik       Date:  1973

7.  Trisomy 12p due to familial t(12p-,6q plus) translocation.

Authors:  J P Fryns; H Van Den Berghe
Journal:  Humangenetik       Date:  1974
  7 in total

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