Literature DB >> 730173

Interstitial deletion of the long arm of chromosome 7 46,XX,del(7)(pter leads to q2200::q3200 leads to qter).

P Franceschini, M C Silengo, G F Davi, M A Santoro, G Prandi, C Fabris.   

Abstract

A newborn girl with multiple anomalies had an interstitial deletion of the long arm of chromosome 7 (46, XX,der(7)mat). The patient's mother and maternal grandmother were carriers of a balanced translocation, 46,XX, inv ins(5;7)(q14;q3200q2200). Both cytogenetic and clinical findings were similar to those in the two cases already described.

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Year:  1978        PMID: 730173     DOI: 10.1007/bf00394300

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


  6 in total

1.  A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).

Authors:  B G Kousseff; L Y Hsu; S Paciuc; K Hirschhorn
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

2.  Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies.

Authors:  G Higginson; D D Weaver; R E Magenis; G H Prescott; C Haag; D J Hepburn
Journal:  Clin Genet       Date:  1976-11       Impact factor: 4.438

3.  7q deletion syndrome (7q32 leads to 7qter).

Authors:  E L Harris; R S Wappner; C G Palmer; B Hall; N Dinno; M R Seashore; W R Breg
Journal:  Clin Genet       Date:  1977-10       Impact factor: 4.438

4.  Deletion of the long arm of chromosome no. 7: tentative assignment of the Kidd (Jk) locus.

Authors:  M H Shokeir; K L Ying; P Pabello
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

5.  Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.

Authors:  J de Grouchy; C Turleau
Journal:  Humangenetik       Date:  1974

6.  [Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].

Authors:  N Ayraud; J Rovinski; J C Lambert; A Galiana
Journal:  Ann Genet       Date:  1976-12
  6 in total
  10 in total

Review 1.  Genetic markers on chromosome 7.

Authors:  L C Tsui
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

2.  Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.

Authors:  K B Nielsen; F Egede; I Mouridsen; J Mohr
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

3.  Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15).

Authors:  E D'Alessandro; C Ligas; M L Lo Re; M P Marcanio; T Gentile; G Del Porto
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

4.  Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32).

Authors:  D N Abuelo; T Padre-Mendoza
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

5.  Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.

Authors:  M D Crawfurd; I Kessel; M Liberman; J A McKeown; P Y Mandalia; M A Ridler
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

6.  A case of partial 5q trisomy associated with partial 7q monosomy.

Authors:  S Hara; T Yamada; H Nakai; A Ohtani; K Mizuno
Journal:  Br J Ophthalmol       Date:  1986-08       Impact factor: 4.638

7.  Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations.

Authors:  M Moller; D García-Cruz; H Rivera; J Sánchez-Corona; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.

Authors:  L Martínez-Jacobo; C Córdova-Fletes; R Ortiz-López; F Rivas; C Saucedo-Carrasco; A Rojas-Martínez
Journal:  Mol Syndromol       Date:  2013-09

9.  Partial monosomy 7q syndrome due to distal interstitial deletion.

Authors:  R Stallard; R C Juberg
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.

Authors:  K Fagan; A Gill; R Henry; I Wilkinson; B Carey
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

  10 in total

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