Literature DB >> 4271166

Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding.

H N Bass, B F Crandall, R S Sparkes.   

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Year:  1973        PMID: 4271166

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


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  17 in total

1.  Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy.

Authors:  P Saldaña-Garcia
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

2.  Familial trisomy 7 mosaicism.

Authors:  L E DeBault; K A Halmi
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

3.  A new contribution to the study of 22 trisomy.

Authors:  A Pérez-Castillo; J A Abrisqueta; M A Martin-Lucas; C Goday; J Del Mazo; V Aller
Journal:  Humangenetik       Date:  1975-09-20

4.  A cytogenetic study of human spontaneous abortions using banding techniques.

Authors:  M R Creasy; J A Crolla; E D Alberman
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

5.  Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.

Authors:  B S Emanuel; E H Zackai; M M Aronson; W J Mellman; P S Moorhead
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

6.  Confirmation of trisomy 22 by trypsin-giemsa staining.

Authors:  M L Begleiter; P Kulkarni; D J Harris
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

7.  47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.

Authors:  E Kessel; R A Pfeiffer
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

8.  Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

Authors:  O Sánchez; J J Yunis
Journal:  Humangenetik       Date:  1974

9.  The aetiology of the cat eye syndrome reconsidered.

Authors:  G Guanti
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

Review 10.  [Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].

Authors:  J Kunze; M Tolksdorf; H R Wiedemann
Journal:  Humangenetik       Date:  1975
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