Literature DB >> 5054320

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

B F Crandall, F Weber, H M Muller, J K Burwell.   

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Year:  1972        PMID: 5054320     DOI: 10.1111/j.1399-0004.1972.tb04275.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  13 in total

1.  Familial Ebstein's anomaly.

Authors:  A Rosenmann; I Arad; A Simcha; T Schaap
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

2.  A case of ring chromosome.

Authors:  D S Brookfield; S Walker
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

3.  Full monosomy 21: a clinically recognizable syndrome?

Authors:  J P Fryns; F D'Hondt; P Goddeeris; H van den Berghe
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

4.  Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysis.

Authors:  R Dalgleish; D P Duckett; M Woodhouse; R S Shannon; I D Young
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

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

Authors:  R J Warren; D L Rimoin; R L Summitt
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

6.  Monozygotic twins with ring chromosome 22.

Authors:  R H Lindenbaum; M Bobrow; L Barber
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

7.  Partial trisomy 14 following a balanced reciprocal translocation t(14q-;21q+).

Authors:  R A Pfeiffer; K Büttinghaus; H Struck
Journal:  Humangenetik       Date:  1973

8.  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

9.  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

10.  A case of r(21) with stigmata of atypical Down syndrome.

Authors:  A Ieshima; N Ogasawara; Y Yamamoto; Y Kuroki
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

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