Literature DB >> 5868696

[Deficiency on the short arms of a chromosome No. 4].

U Wolf, H Reinwein, R Porsch, R Schröter, H Baitsch.   

Abstract

Mesh：

Year:  1965        PMID： 5868696

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


× No keyword cloud information.
  13 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.  DELETION OF THE SHORT ARM OF CHROMOSOME 18.

Authors:  R L SUMMITT
Journal:  Cytogenetics       Date:  1964

3.  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

4.  DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.

Authors:  W SCHMID
Journal:  Cytogenetics       Date:  1963

5.  [3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].

Authors:  J LEJEUNE; J LAFOURCADE; R BERGER; J VIALATTE; M BOESWILLWALD; P SERINGE; R TURPIN
Journal:  C R Hebd Seances Acad Sci       Date:  1963-11-18

6.  CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.

Authors:  J GERMAN; J LEJEUNE; M N MACINTYRE; J DE GROUCHY
Journal:  Cytogenetics       Date:  1964

7.  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

8.  Deficiency.

Authors:  C B Bridges
Journal:  Genetics       Date:  1917-09       Impact factor: 4.562

9.  [Offsprings of balanced fusion and translocation heterozygotes].

Authors:  G R Stalder; E M Bühler; U K Bühler
Journal:  Helv Paediatr Acta       Date:  1965-06

10.  Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

Authors:  K Hirschhorn; H L Cooper; I L Firschein
Journal:  Humangenetik       Date:  1965
View more
  59 in total

1.  C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development.

Authors:  Sabine Endele; Claudia Nelkenbrecher; Annegret Bördlein; Stefanie Schlickum; Andreas Winterpacht
Journal:  Neurogenetics       Date:  2011-02-02       Impact factor: 2.660

2.  A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.

Authors:  J Goodship; A Curtis; I Cross; J Brown; J Emslie; J Wolstenholme; S Bhattacharya; J Burn
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

Review 3.  Wolf syndrome.

Authors:  D S Katz; T H Smith
Journal:  Pediatr Radiol       Date:  1991

4.  Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements.

Authors:  Yue Luo; Karen E Hermetz; Jodi M Jackson; Jennifer G Mulle; Anne Dodd; Karen D Tsuchiya; Blake C Ballif; Lisa G Shaffer; Jannine D Cody; David H Ledbetter; Christa L Martin; M Katharine Rudd
Journal:  Hum Mol Genet       Date:  2011-07-04       Impact factor: 6.150

5.  Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.

Authors:  S K Shapira; C McCaskill; H Northrup; A S Spikes; F F Elder; V R Sutton; J R Korenberg; F Greenberg; L G Shaffer
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

6.  Ring chromosome 4 and Wolf syndrome.

Authors:  A Pérez-Castillo; J A Abrisqueta
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

7.  Prenatal recognition of 4p- syndrome.

Authors:  S Blunt; A C Berry; M J Seller; C A Williams
Journal:  J Med Genet       Date:  1977-06       Impact factor: 6.318

8.  Familial Wolf-Hirschhorn syndrome resulting from a cryptic translocation: a clinical and molecular study.

Authors:  E Reid; N Morrison; L Barron; E Boyd; A Cooke; D Fielding; J L Tolmie
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

9.  Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm.

Authors:  Danielle A Callaway; Ian M Campbell; Samantha R Stover; Andres Hernandez-Garcia; Shalini N Jhangiani; Jaya Punetha; Ingrid S Paine; Jennifer E Posey; Donna Muzny; Kevin P Lally; James R Lupski; Chad A Shaw; Caraciolo J Fernandes; Daryl A Scott
Journal:  J Pediatr Genet       Date:  2018-05-30

Review 10.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

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

北京卡尤迪生物科技股份有限公司 © 2022-2023.