Literature DB >> 4865216

[On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

K Bender, H Ritter, U Wolf.   

Abstract

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Year:  1967        PMID： 4865216     DOI： 10.1007/BF00291253

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


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  75 in total

1.  THE "CAT CRY" SYNDROME.

Authors:  M N MACINTYRE; W I STAPLES; J LAPOLLA; J M HEMPEL
Journal:  Am J Dis Child       Date:  1964-11

2.  [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

3.  GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME.

Authors:  N J BRANDT; A FROLAND; M MIKKELSEN; A NIELSEN; N TOLSTRUP
Journal:  Lancet       Date:  1963-10-05       Impact factor: 79.321

4.  [FAMILIAL AND ANEUPLOID MARKER CHROMOSOMES. POSSIBLE ROLE OF CHROMOSOME INTERACTION].

Authors:  J DE GROUCHY; S THIEFFRY; M ARTHUIS; J GERBEAUX; S POUPINET; C SALMON; M LAMY
Journal:  Ann Genet       Date:  1964

5.  "CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY.

Authors:  J S MCCRACKEN; R R GORDON
Journal:  Lancet       Date:  1965-01-02       Impact factor: 79.321

6.  PHENOTYPIC SHIFTS IN TRISOMY.

Authors:  H O GOODMAN
Journal:  Am J Hum Genet       Date:  1965-03       Impact factor: 11.025

7.  FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors:  I A UCHIDA; K N MCRAE; M RAY
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

8.  The leucocyte alkaline phosphatase in mongolism.

Authors:  S TRUBOWITZ; D KIRMAN; B MASEK
Journal:  Lancet       Date:  1962-09-08       Impact factor: 79.321

9.  [Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].

Authors:  C Laurent; J M Robert
Journal:  Ann Genet       Date:  1966-09

10.  [Studies on the activity of galactokinase in the blood of normal persons and of patients with GDo trisomy].

Authors:  W Krone; U Wolf; H W Goedde; H Baitsch
Journal:  Humangenetik       Date:  1965
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  9 in total

1.  Exclusion of the localization of the Gm, Pi, and C3 genes on 6q25 to 6qter through blood group analysis of the patients of Schmid, D'Apuzzo and Rossi (Hum. Genet. 46, 279--284, 1979.

Authors:  K Bender; K Burckhardt; K Schroetter
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

Review 2.  Utilization of somatic cell hybrids for genetic studies in man.

Authors:  K H Grzeschik
Journal:  Humangenetik       Date:  1973

3.  [Enzyme analysis in serum of feeble minded hospitalized patients].

Authors:  F Schweikhardt; P Grünwald
Journal:  Humangenetik       Date:  1968

4.  Red cell enzymes in trisomy 21.

Authors:  S N Pantelakis; A G Karaklis; D Alexiou; E Vardas; T Valaes
Journal:  Am J Hum Genet       Date:  1970-03       Impact factor: 11.025

Review 5.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

6.  [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

7.  [On the problem of loci order. II. Localization by 5p deficiencies].

Authors:  W Engel; J Op't Hof; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1968

8.  Human chromosomal deficiency: the 4p--syndrome.

Authors:  E Passarge; H C Altrogge; R A Rüdiger
Journal:  Humangenetik       Date:  1970-08-17

9.  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
  9 in total

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