Literature DB >> 7154046

Recurrent spontaneous abortions due to a homologous Robertsonian translocation (14q14q).

R Gracias-Espinal, S H Roberts, D P Duckett, K M Laurence.   

Abstract

Mesh:

Year:  1982        PMID: 7154046      PMCID: PMC1048965          DOI: 10.1136/jmg.19.6.465

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  17 in total

1.  [Identification by Q and G bands of chromosome anomalies in spontaneous abortion].

Authors:  J Boué; M J Daketsé; C Deluchat; N Ravisé; F Yvert; A Boué
Journal:  Ann Genet       Date:  1976-12

2.  Translocation D/D involving two homologous chromosomes of the pair 15.

Authors:  J Zizka; P Balícek; A Finková
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

3.  Recurrent abortion associated with a balanced 22;22 translocation, or isochromosome 22q in a monozygous twin.

Authors:  B V Lewis; M A Ridler
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

4.  Giemsa banding in the t(13q13q) carrier mother of a translocation trisomy 13 abortus.

Authors:  M I Parslow; R J Gardner; A M Veale
Journal:  Humangenetik       Date:  1973-04-16

5.  Recurrent abortions and chromosome abnormalities.

Authors:  M Lucas; I Wallace; K Hirschhorn
Journal:  J Obstet Gynaecol Br Commonw       Date:  1972-12

6.  Sibship (21q21q) translocation Down's syndrome with maternal transmission.

Authors:  M Furbetta; A Falorni; P Antignani; A Cao
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

7.  The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography.

Authors:  M M Cohen
Journal:  Ann Genet       Date:  1971-06

8.  [Trisomy D2 in a 2 and one-half year old girl (47,XX,14+)].

Authors:  J D Murken; M Bauchinger; D Palitzsch; H Pfeifer; J Suschke; H Haendle
Journal:  Humangenetik       Date:  1970

9.  Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis.

Authors:  T Caspersson; M Hultén; J Lindsten; A J Therkelsen; L Zech
Journal:  Hereditas       Date:  1971       Impact factor: 3.271

10.  A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.

Authors:  J L Hamerton; N Canning; M Ray; S Smith
Journal:  Clin Genet       Date:  1975-10       Impact factor: 4.438

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  3 in total

1.  Homologous Robertsonian translocation (21q21q) and abortions.

Authors:  T Sudha; P M Gopinath
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

Review 2.  Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements.

Authors:  D Kotzot
Journal:  J Med Genet       Date:  2001-08       Impact factor: 6.318

3.  Maternal uniparental isodisomy of chromosome 14: association with autosomal recessive rod monochromacy.

Authors:  L Pentao; R A Lewis; D H Ledbetter; P I Patel; J R Lupski
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

  3 in total

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