Literature DB >> 22622526

A rare chromosomal abnormality inherited from the mother in a boy conceived after intracytoplasmic sperm injection: a case report.

Li Yin1, Hong Tian, Long-jie Gu, Ding Ma, Han-wang Zhang, Gui-jin Zhu.   

Abstract

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Year:  2012        PMID： 22622526      PMCID： PMC3463672          DOI： 10.1007/s10815-012-9796-9

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN： 1058-0468            Impact factor:   3.412


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  14 in total

1.  Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing.

Authors:  O Henegariu; N A Heerema; L Lowe Wright; P Bray-Ward; D C Ward; G H Vance
Journal:  Cytometry       Date:  2001-02-01

2.  Molecular characterization and delineation of subtle deletions in de novo "balanced" chromosomal rearrangements.

Authors:  A Kumar; L A Becker; T W Depinet; J M Haren; C L Kurtz; N H Robin; S B Cassidy; D J Wolff; S Schwartz
Journal:  Hum Genet       Date:  1998-08       Impact factor: 4.132

3.  Tandem duplication of the terminal band of the long arm of chromosome 7 (dir dup (7)(q36----qter)).

Authors:  R S Verma; R A Conte; J H Pitter
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

4.  Chromosome translocations in couples with in-vitro fertilization implantation failure.

Authors:  C Stern; M Pertile; H Norris; L Hale; H W Baker
Journal:  Hum Reprod       Date:  1999-08       Impact factor: 6.918

5.  Structural organization of the human short-chain acyl-CoA dehydrogenase gene.

Authors:  M J Corydon; B S Andresen; P Bross; M Kjeldsen; P H Andreasen; H Eiberg; S Kølvraa; N Gregersen
Journal:  Mamm Genome       Date:  1997-12       Impact factor: 2.957

Review 6.  Chromosome abnormalities in human beings.

Authors:  D E McFadden; J M Friedman
Journal:  Mutat Res       Date:  1997-12-12       Impact factor: 2.433

7.  Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.

Authors:  C P Chen; K Devriendt; C C Lee; W L Chen; W Wang; T Y Wang
Journal:  Prenat Diagn       Date:  1999-10       Impact factor: 3.050

8.  A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.

Authors:  Alicia Vaglio; Aubrey Milunsky; Xin-Li Huang; Andrea Quadrelli; Búrix Mechoso; Roberto Quadrelli
Journal:  Eur J Med Genet       Date:  2007-01-21       Impact factor: 2.708

9.  A girl with partial trisomy 12q24.31 inherited from her father and a possible novel syndrome transmitted from her mother.

Authors:  Liming Bao; Elizabeth K Schorry
Journal:  Am J Med Genet A       Date:  2005-11-01       Impact factor: 2.802

10.  Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin.

Authors:  Ingrid Tein; Orly Elpeleg; Bruria Ben-Zeev; Stanley H Korman; Alexander Lossos; Dorit Lev; Tally Lerman-Sagie; Esther Leshinsky-Silver; Jerry Vockley; Gerard T Berry; Anne-Marie Lamhonwah; Dietrich Matern; Charles R Roe; Niels Gregersen
Journal:  Mol Genet Metab       Date:  2007-12-03       Impact factor: 4.797
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