Literature DB >> 2633989

Indications for cytogenetic studies.

Q H Qazi.   

Abstract

Mesh：

Year:  1989        PMID： 2633989     DOI： 10.1007/bf02722412

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  8 in total

Review 1.  The prenatal detection of the fragile X chromosome: review of recent experience.

Authors:  E C Jenkins; W T Brown; M G Wilson; M S Lin; O S Alfi; E R Wassman; J Brooks; C J Duncan; A Masia; M S Krawczun
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

2.  Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses.

Authors:  M A Ferguson-Smith; J R Yates
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

Review 3.  New concepts and questions in gestational trophoblastic disease.

Authors:  M G Dodson
Journal:  J Reprod Med       Date:  1983-11       Impact factor: 0.142

4.  A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

Authors:  A Boué; P Gallano
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

5.  Risk for chromosome abnormality at amniocentesis following a child with a non-inherited chromosome aberration. A European Collaborative Study on Prenatal Diagnoses 1981.

Authors:  J Stene; E Stene; M Mikkelsen
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

6.  Chromosome studies in 496 infertile males with a sperm count below 10 million/ml.

Authors:  A E Retief; J A Van Zyl; R Menkveld; M F Fox; G M Kotzè; J Brusnickỳ
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Chromosomal findings in 164 couples with repeated spontaneous abortions: with special consideration to prior reproductive history.

Authors:  S Schwartz; C G Palmer
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

8.  The SC phocomelia syndrome: report of two cases with cytogenetic abnormality.

Authors:  Q H Qazi; E G Kassner; A Masakawa; C Madahar; S J Choi
Journal:  Am J Med Genet       Date:  1979
  8 in total

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