Literature DB >> 4541805

Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.

O Alfi, G N Donnell, B F Crandall, A Derencsenyi, R Menon.   

Abstract

Mesh：

Year:  1973        PMID： 4541805

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  35 in total

1.  Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Authors:  L A Christ; C A Crowe; M A Micale; J M Conroy; S Schwartz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.

Authors:  U Francke; C Kernahan; C Bradshaw
Journal:  Humangenetik       Date:  1975

Review 3.  Genetic mechanisms underlying male sex determination in mammals.

Authors:  R P Piprek
Journal:  J Appl Genet       Date:  2009       Impact factor: 3.240

4.  A case of 9p- syndrome.

Authors:  Y Kuroki; S Yokota; H Nakai; Y Yamamoto; I Matsui
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

Review 5.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

6.  Mental retardation and congenital malformations associated with a ring chromosome 9.

Authors:  S Nakajima; M Yanagisawa; S Kamoshita; Y Nakagome
Journal:  Hum Genet       Date:  1976-06-29       Impact factor: 4.132

7.  Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.

Authors:  Érika L Freitas; Susan M Gribble; Milena Simioni; Társis P Vieira; Roseane L Silva-Grecco; Marly A S Balarin; Elena Prigmore; Ana C Krepischi-Santos; Carla Rosenberg; Karoly Szuhai; Arie van Haeringen; Nigel P Carter; Vera Lúcia Gil-da-Silva-Lopes
Journal:  Am J Med Genet A       Date:  2011-09-21       Impact factor: 2.802

Review 8.  Familial translocation t(9;16).

Authors:  C Dowman; D Lockwood; J Allanson
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

9.  A girl with karyotype 46,XX,del(7)(qter-p 15:).

Authors:  U Friedrich; T Lyngbye; J Oster
Journal:  Humangenetik       Date:  1975

10.  A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice.

Authors:  Jian Zhou; John R McCarrey; P Jeremy Wang
Journal:  Biol Reprod       Date:  2013-06-27       Impact factor: 4.285
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