Literature DB >> 5449951

[Elongated, submetacentric chromosome no. 1. A very rare heterozygote variant in man].

B Saner.   

Abstract

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Year:  1970        PMID： 5449951     DOI： 10.1007/bf00297641

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  24 in total

1.  Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.

Authors:  J J YUNIS; R J GORLIN
Journal:  Chromosoma       Date:  1963       Impact factor: 4.316

2.  The sites and relative frequencies of secondary constrictions in human somatic chromosomes.

Authors:  M A FERGUSON-SMITH; M E FERGUSON-SMITH; P M ELLIS; M DICKSON
Journal:  Cytogenetics       Date:  1962

3.  Hypertrophied frenuli, oligophrenia, famflial trembling and anomalies of the hand. Report of four casesin one family and a forme fruste in another.

Authors:  R J GORLIN; V E ANDERSON; C R SCOTT
Journal:  N Engl J Med       Date:  1961-03-09       Impact factor: 91.245

4.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

5.  The oral-facial-digital syndrome: a multiple congenital condition of females with associated chromosomal abnormalities.

Authors:  A L RUESS; S PRUZANSKY; E F LIS; K PATAU
Journal:  Pediatrics       Date:  1962-06       Impact factor: 7.124

6.  Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.

Authors:  K PATAU; E THERMAN; S L INHORN; D W SMITH; A L RUESS
Journal:  Chromosoma       Date:  1961       Impact factor: 4.316

7.  Enlarged chromosome No. 1 in a patient with primary amenorrhoea.

Authors:  J Philip; O Frydenberg; V Sele
Journal:  Cytogenetics       Date:  1965

Review 8.  [Karyotype and phenotype of autosome aberrations in man].

Authors:  R A Pfeiffer
Journal:  Veroff Morphol Pathol       Date:  1968

9.  Chronology and pattern of human chromosome replication. VI. Further studies including autoradiographic behavior of normal and abnormal no. 1 autosomes.

Authors:  T Sofuni; A A Sandberg
Journal:  Cytogenetics       Date:  1967

10.  Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases.

Authors:  C E BLANK
Journal:  Ann Hum Genet       Date:  1960-05       Impact factor: 1.670
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  1 in total

1.  Frequency and genetic effect of 1qh plus.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson
Journal:  Humangenetik       Date:  1974-02-21
  1 in total

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