Literature DB >> 5915640

[Deletion of the short arms of chromosome No. 18].

R A Pfeiffer.   

Abstract

Mesh：

Year:  1966        PMID： 5915640     DOI： 10.1007/bf00291517

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


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  11 in total

1.  [FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"].

Authors:  J LEJEUNE; J LAFOURCADE; R BERGER; R TURPIN
Journal:  C R Hebd Seances Acad Sci       Date:  1964-06-08

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.  MULTIPLE CONGENITAL ANOMALIES ASSOCIATED WITH A PARTIALLY RING-SHAPED CHROMOSOME PROBABLY DERIVED FROM CHROMOSOME NO. 18 IN MAN.

Authors:  A GROPP; A JUSSEN; K OFTERINGER
Journal:  Nature       Date:  1964-05-23       Impact factor: 49.962

4.  DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Authors:  R L SUMMITT
Journal:  Cytogenetics       Date:  1964

5.  TRANSLOCATION IN THE 13-15 GROUP AS A CAUSE OF PARTIAL TRISOMY AND SPONTANEOUS ABORTION IN THE SAME FAMILY.

Authors:  P JACOBSEN; A DUPONT; M MIKKELSEN
Journal:  Lancet       Date:  1963-09-14       Impact factor: 79.321

6.  A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.

Authors:  K H GUSTAVSON; S C FINLEY; W H FINLEY; B JALLING
Journal:  Acta Paediatr       Date:  1964-03       Impact factor: 2.299

7.  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

8.  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

9.  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

10.  Cebocephaly with endocrine dysgenesis. Report of 3 cases.

Authors:  J C HAWORTH; H MEDOVY; A J LEWIS
Journal:  J Pediatr       Date:  1961-11       Impact factor: 4.406
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  8 in total

Review 1.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

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

Review 2.  Partial monosomies 18. Review of cytogenetical and phenotypical variants.

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

Review 3.  [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

4.  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

5.  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

6.  Deletion of short arm of a chromosome 18 (46, XX, 18 p-).

Authors:  H Reinwein; H Ritter; U Wolf
Journal:  Humangenetik       Date:  1967-11-29

7.  The 18 p-syndrome. Report of four cases.

Authors:  J Faust; M Habedank; C Nieuwenhuijsen
Journal:  Eur J Pediatr       Date:  1976-08-16       Impact factor: 3.183

8.  Chromosomal abnormalities associated with cyclopia and synophthalmia.

Authors:  R O Howard
Journal:  Trans Am Ophthalmol Soc       Date:  1977
  8 in total

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