Literature DB >> 4116769

Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication.

J R Lobitz, B K McCaw, F Hecht.   

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Year:  1972        PMID： 4116769      PMCID： PMC1469145          DOI： 10.1136/jmg.9.3.276

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


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  16 in total

1.  Chromosome polymorphism in American Negro and White populations.

Authors:  H A Lubs; F H Ruddle
Journal:  Nature       Date:  1971-09-10       Impact factor: 49.962

2.  A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.

Authors:  H L COOPER; R HERNITS
Journal:  Am J Hum Genet       Date:  1963-12       Impact factor: 11.025

3.  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

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.  Genetic Control of Hemoglobin Synthesis.

Authors:  W E Nance
Journal:  Science       Date:  1963-07-12       Impact factor: 47.728

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.  Location of satellite and homogeneous DNA sequences on human chromosomes.

Authors:  K W Jones; G Corneo
Journal:  Nat New Biol       Date:  1971-10-27

8.  New technique for distinguishing between human chromosomes.

Authors:  A T Sumner; H J Evans; R A Buckland
Journal:  Nat New Biol       Date:  1971-07-07

9.  Possible linkage between uncoiler chromosome Un 1 and amylase polymorphism Amy 2 loci.

Authors:  J Kamarýt; R Adámek; M Vrba
Journal:  Humangenetik       Date:  1971

10.  Polymorphism of human constitutive heterochromatin.

Authors:  A P Craig-Holmes; M W Shaw
Journal:  Science       Date:  1971-11-12       Impact factor: 47.728
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  9 in total

1.  Classification of qh regions in human chromosomes 1, 9, and 16 by C-banding.

Authors:  S R Patil; H A Lubs
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

2.  Frequency and genetic effect of 1qh plus.

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

3.  Cytogenetic and linkage studies of a familial 15pplus variant.

Authors:  F E Yoder; W B Bias; D S Borgaonkar; G F Bahr; I I Yoder; O C Yoder; H M Golomb
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

4.  [Polymorphism of human constitutive heterochromatin in metaphase chromosome A1].

Authors:  M A Kim
Journal:  Humangenetik       Date:  1973-05-25

5.  Annotation: genetic effects of aneuploidy.

Authors:  L Sandler; F Hecht
Journal:  Am J Hum Genet       Date:  1973-05       Impact factor: 11.025

6.  Giemsa banding of chromosome 1gh+ and linkage analysis.

Authors:  P N Howard; G R Stoddard; M W Goddard; J R Seely
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

7.  Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements.

Authors:  C S Lee; K L Ying; P Bowen
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

8.  1q plus variants in a normal adult population (one with a pericentric inversion).

Authors:  S Tüür; M Käosaar; A V Mikelsaar
Journal:  Humangenetik       Date:  1974

9.  Minor chromosome variations and selected heteromorphisms in 200 unclassifiable mentally retarded patients and 200 normal controls.

Authors:  A T Tharapel; R L Summitt
Journal:  Hum Genet       Date:  1978-03-17       Impact factor: 4.132
  9 in total

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