Literature DB >> 14207551

PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18.

H E VANDYKE, A VALDMANIS, J D MANN.   

Abstract

Keywords:  17-KETOSTEROIDS; ADOLESCENCE; ADRENAL CORTEX HORMONES; BLOOD GROUPS; CHROMOSOME ABNORMALITIES; ESTROGENS; GONADOTROPINS, PITUITARY; HAPTOGLOBINS; MENTAL RETARDATION; TRANSFERRIN; URINE

Mesh：

Substances：

Year:  1964        PMID： 14207551      PMCID： PMC1932472     

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


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  15 in total

1.  A NEW TRISOMY-TRANSLOCATION CHROMOSOME (LONG-ARM E/E).

Authors:  R A ROHDE; A LEE; S SAPIN
Journal:  Lancet       Date:  1963-12-21       Impact factor: 79.321

2.  PRESUMED TRANSLOCATION OF CHROMOSOME NUMBER 2 AND ONE OF THE D GROUP.

Authors:  R D MERCER; G DARAKJIAN
Journal:  Cleve Clin Q       Date:  1963-10

3.  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

4.  The No. 18 trisomy syndrome.

Authors:  D W SMITH; K PATAU; E THERMAN; S L INHORN
Journal:  J Pediatr       Date:  1962-04       Impact factor: 4.406

5.  Familial translocation mongolism: a carrier exhibiting nonacrocentric translocation.

Authors:  K BECKER; A ALBERT
Journal:  Proc Staff Meet Mayo Clin       Date:  1963-06-19

6.  An abnormal chromosome in chronic lymphocytic leukaemia.

Authors:  F W GUNZ; P H FITZGERALD; A ADAMS
Journal:  Br Med J       Date:  1962-10-27

7.  The E syndrome (trisomy 17-18) resulting from a maternal chromosomal translocation.

Authors:  H R BRODIE; L DALLAIRE
Journal:  Can Med Assoc J       Date:  1962-09-08       Impact factor: 8.262

8.  An XYY man with progeny indicating familial tendency to non-disjunction.

Authors:  T S HAUSCHKA; J E HASSON; M N GOLDSTEIN; G F KOEPF; A A SANDBERG
Journal:  Am J Hum Genet       Date:  1962-03       Impact factor: 11.025

9.  Cytogenetic studies in primary amenorrhoea.

Authors:  P A JACOBS; D G HARNDEN; K E BUCKTON; W M BROWN; M J KING; J A McBRIDE; T N MACGREGOR; N MACLEAN
Journal:  Lancet       Date:  1961-06-03       Impact factor: 79.321

10.  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
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  16 in total

1.  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

Review 2.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

Review 3.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors:  I W Lurie; G I Lazjuk
Journal:  Humangenetik       Date:  1972

Review 4.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

Review 5.  [On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].

Authors:  K Bender; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1967

6.  Double satellites: autoradiographic study of a chromosomal marker observed in two generations.

Authors:  A Rocchi; A De Capoa; F Gigliani
Journal:  Humangenetik       Date:  1971

7.  Arrhinencephaly associated with a deficiency involving chromosome 18.

Authors:  A McDermott; J Insley; M E Barton; P Roowe; J H Edwards; A H Cameron
Journal:  J Med Genet       Date:  1968-03       Impact factor: 6.318

8.  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.  Absent IgA and deletions of chromosome 18.

Authors:  J M Stewart; S Go; E Ellis; A Robinson
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318

10.  Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum.

Authors:  P Fischer; E Golob; F Friedrich; E Kunze-Mühl; W Doleschel; H Aichmair
Journal:  J Med Genet       Date:  1970-03       Impact factor: 6.318
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