Literature DB >> 6949855

Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].

M G Wilson, J W Towner, G S Coffin, A J Ebbin, E Siris, P Brager.   

Abstract

Clinical and cytogenetic studies are reported on 13 patients with Wolf-Hirschhorn syndrome. The oldest of the living twelve probands is 24 years of age. Three of these patients had a translocation involving the short arm of chromosome 4, and in one of these the anomalous chromosome was inherited from the father. Another three patients were believed, on the basis of GTG-staining, to have a translocation although the origin of the translocated chromatin could not be identified. In the remaining seven patients the anomalous chromosome appeared to be a simple deletion, although in two cases a translocation could not be ruled out. Cytogenetic studies in these patients suggest that the critical deletion involved in Wolf-Hirschhorn syndrome is within 4p16.

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Year:  1981        PMID: 6949855     DOI: 10.1007/bf00295461

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  35 in total

1.  4p- phenotype in an infant with t(4p-;19p or q+)mat translocation.

Authors:  R L Neu; R J Shott; L I Gardner
Journal:  Am J Dis Child       Date:  1975-03

2.  A 13-year-old girl with Wolf's syndrome and karyotype 46,XX,del(4)(pter integral p15::p12 integral qter),9qh+. Increased risk of structural chromosome abnormalities in the progeny of mothers with 9qh+.

Authors:  J Nielsen; O Fischer; K Rasmussen; I Sillesen; A Bernsen; P Saldaña-Garcia
Journal:  J Ment Defic Res       Date:  1977-06

3.  Wolf-Hirschhorn syndrome and balanced (4;10) translocation in the father.

Authors:  K Hedner; E Carlsson; F Mitelman
Journal:  Clin Genet       Date:  1977-08       Impact factor: 4.438

4.  Ring chromosome 4 and Wolf syndrome.

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

5.  [Partial trisomy 10p of paternal origin. 2 new cases in 2 different families].

Authors:  M Rolland; G Bourrouillou; G Elana; P Colombies; C Regnier
Journal:  Ann Genet       Date:  1977-09

6.  [Partial deletion of the short arm of chromosome 4. Apropos of 3 cases].

Authors:  J L Taillemite; G Tufferaud; P Hazael-Massieux; G Baheux-Morlier; C Roux
Journal:  Ann Genet       Date:  1977-06

7.  A syndrome of retarded development with characteristic appearance.

Authors:  G S Coffin
Journal:  Am J Dis Child       Date:  1968-06

8.  Deletion of the short arm of chromosome 4 from a subject with Wolf's syndrome. Repository identification no. GM-72.

Authors:  W R Breg; M M Aronson; A E Greene; L L Coriell
Journal:  Cytogenet Cell Genet       Date:  1977

9.  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

10.  Trisomy 4p and deletion 4p- in a family having translocation, t(4p-; 12p+).

Authors:  J G Mortimer; W Chewings; P Miethke; G F Smith
Journal:  Hum Hered       Date:  1978       Impact factor: 0.444

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  20 in total

1.  A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

Authors:  L L Estabrooks; A N Lamb; H N Kirkman; N P Callanan; K W Rao
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

2.  Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Authors:  H S Stadler; B J Padanilam; K Buetow; J C Murray; M Solursh
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

3.  Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome.

Authors:  M W Partington; K Fagan; V Soubjaki; G Turner
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

4.  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

5.  Dissecting the Wolf-Hirschhorn syndrome phenotype: WHSC1 is a neurodevelopmental gene contributing to growth delay, intellectual disability, and to the facial dysmorphism.

Authors:  Marcella Zollino; Paolo Niccolo' Doronzio
Journal:  J Hum Genet       Date:  2018-06-08       Impact factor: 3.172

6.  Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4.

Authors:  C McKeown; A P Read; A Dodge; O Stecko; A Mercer; R Harris
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

7.  Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Authors:  L L Estabrooks; A N Lamb; A S Aylsworth; N P Callanan; K W Rao
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318

8.  Trisomy 4p and ocular defects.

Authors:  I W Lurie; V A Samochvalov
Journal:  Br J Ophthalmol       Date:  1994-05       Impact factor: 4.638

9.  Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.

Authors:  M Anvret; M Nordenskjöld; L Stolpe; L Johansson; K Bröndum-Nielsen
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

10.  Molecular definition of the smallest region of deletion overlap in the Wolf-Hirschhorn syndrome.

Authors:  K Y Gandelman; L Gibson; M S Meyn; T L Yang-Feng
Journal:  Am J Hum Genet       Date:  1992-09       Impact factor: 11.025

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