Literature DB >> 4265215

Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

R J Warren, D L Rimoin, R L Summitt.   

Abstract

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Year:  1973        PMID： 4265215      PMCID： PMC1762232     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  11 in total

1.  [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

Authors:  J LEJEUNE; R BERGER; M O RETHORE; L ARCHAMBAULT; H JEROME; S THIEFFRY; J AICARDI; M BROYER; J LAFOURCADE; J CRUVEILLER; R TURPIN
Journal:  C R Hebd Seances Acad Sci       Date:  1964-11-30

2.  Ring-G chromosome, a new G-deletion syndrome?

Authors:  R G Weleber; F Hecht; E R Giblett
Journal:  Am J Dis Child       Date:  1968-04

3.  [Ring G-chromosome. Report of two cases and review of literature].

Authors:  K P Grosse; B Böwing; F Hopfengärtner; G Reinhardt; C F Sitzmann
Journal:  Humangenetik       Date:  1971

4.  G-group ring chromosome in a mentally subnormal girl.

Authors:  B W Richards; A T Rundle; W M Hatton; A Stewart
Journal:  J Ment Defic Res       Date:  1971-03

5.  Identification of 21r and 22r chromosomes by quinacrine fluorescence.

Authors:  B F Crandall; F Weber; H M Muller; J K Burwell
Journal:  Clin Genet       Date:  1972       Impact factor: 4.438

6.  G-deletion syndrome II.

Authors:  P J Chauvel; J D Schindeler; R J Warren
Journal:  Humangenetik       Date:  1972

7.  Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.

Authors:  S Armendares; L Buentello; J M Cantu-Garza
Journal:  Ann Genet       Date:  1971-03

8.  [The Dr phenotype: a study of threee cases with a ring D chromosome].

Authors:  J Lejeune; J Lafourcade; R Berger; J Cruveiller; M O Rethoré; B Dutrillaux; D Abonyi; H Jérôme
Journal:  Ann Genet       Date:  1968-06

9.  The G deletion syndromes.

Authors:  R J Warren; D L Rimoin
Journal:  J Pediatr       Date:  1970-10       Impact factor: 4.406

10.  DNA-binding fluorochromes for the study of the organization of the metaphase nucleus.

Authors:  T Caspersson; L Zech; E J Modest; G E Foley; U Wagh; E Simonsson
Journal:  Exp Cell Res       Date:  1969-11       Impact factor: 3.905
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  16 in total

1.  A male infant with monosomy 21.

Authors:  Y Kaneko; T Ikeuchi; M Sasaki; Y Stakae; S Kuwajima
Journal:  Humangenetik       Date:  1975-08-29

2.  Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).

Authors:  D R Romain; J Goldsmith; H Cairney; L M Columbano-Green; R H Smythe; R G Parfitt
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

3.  Balanced translocation, impaired sperm motility, and offspring anomaly.

Authors:  J R Oakley; P Else; P Asplin; L S Taitz
Journal:  Arch Dis Child       Date:  1976-08       Impact factor: 3.791

4.  A female infant with monosomy 21.

Authors:  P Dziuba; D Dziekanowska; H Hübner
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

5.  Long arm deletion of chromosome 22.

Authors:  G Kirshenbaum; M Chmura; D P Rhone
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

6.  Clinical and cytogenetic studies of two infants with partial monosomy G.

Authors:  T Maeda; M Ohno; H Nishida
Journal:  Hum Genet       Date:  1977-03-14       Impact factor: 4.132

7.  Four new cases of ring 21 and 22 including familial transmission of ring 21.

Authors:  C G Palmer; M E Hodes; T Reed; J Kojetin
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

8.  Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit?

Authors:  J L García Miranda; A Otero Gómez; H Varela Ansedes; N Rancel Torres; C González Espinosa; C Cortabarría; G Sánchez Salgado
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

9.  Partial monosomy 13 and 21 due to a familial 13/21 translocation.

Authors:  P G Otto; S Toledo; A Richieri-Costa; P A Otto; A M Vianna-Morgante; S Kasahara
Journal:  Hum Genet       Date:  1978-04-24       Impact factor: 4.132

10.  Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.

Authors:  M Mikkelsen; S Vestermark
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318
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