Literature DB >> 4135065

[Inherited translocation t(4q minus;18q plus) with unbalanced progeny of different types (author's transl)].

H Knörr-Gärtner, K Knörr, B Haas, W Vogel, J W Siebers.   

Abstract

Mesh：

Year:  1974        PMID： 4135065

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  10 in total

1.  A rapid banding technique for routine use in human and comparative cytogenetics.

Authors:  K Sperling; R Wiesner
Journal:  Humangenetik       Date:  1972

2.  Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining.

Authors:  M Mikkelsen
Journal:  Humangenetik       Date:  1971

3.  [A case of a possible tandem-translocation C-13 in a boy with malformations].

Authors:  W Vogel; H Reinwein; W Engel
Journal:  Z Kinderheilkd       Date:  1971

4.  Prenatal diagnosis of chromosome abnormalities.

Authors:  A J Therkelsen; G B Petersen; O R Steenstrup; J Jonasson; J Lindsten; L Zech
Journal:  Acta Paediatr Scand       Date:  1972-07

5.  [On pregnancies with a genetic high risk (technique, indications and results of genetic amniocentesis) (author's transl)].

Authors:  K Knörr; W D Jonatha; H Knörr-Gärtner
Journal:  Geburtshilfe Frauenheilkd       Date:  1973-08       Impact factor: 2.915

6.  A modified method of culturing human amniotic fluid cells for prenatal detection of genetic disorders.

Authors:  H Knörr-Gärtner; I Härle
Journal:  Humangenetik       Date:  1972

7.  [Complex chromosome changes bearing on the autosomes accompanying cranio-facial abnormalities and an umbilical hernia].

Authors:  J Ruffié; J Virenque; A Bardier; P Colombies
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1966-01-17

8.  Aneusomie de recombinaison: rearrangement between paternal chromosomes 4 and 18 yielding offspring with features of the 18q- syndrome.

Authors:  H Hoehn; C Sander; L Z Sander
Journal:  Ann Genet       Date:  1971-09

9.  [On two familial cases of complex translocations].

Authors:  J Lejeune; R Burger
Journal:  Ann Genet       Date:  1965

10.  Mitotic and meiotic studies of a familial reciprocal translocation between autosomes 15 and 18 in man.

Authors:  K Fredga; S Rayner
Journal:  Hereditas       Date:  1967       Impact factor: 3.271
  10 in total
  8 in total

1.  Meiotic chromosome study in a human female translocation heterozygote.

Authors:  B U Kallhardt; K Knörr
Journal:  Humangenetik       Date:  1975

2.  Translocation +(7p+; Bq-) associated with recurrent abortion.

Authors:  H Körner; H Agricola; H Bayer
Journal:  Humangenetik       Date:  1975-05-26

3.  Nonrandom distribution of exchange points in patients with structural rearrangements.

Authors:  Y Nakagome; H Chiyo
Journal:  Am J Hum Genet       Date:  1976-01       Impact factor: 11.025

4.  Partial trisomy 4q: two cases with a familial translocation t(4;18)(q27;q23).

Authors:  M Stella; A Bonfante; G Ronconi; G Rossi
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

5.  Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).

Authors:  C Fonatsch; S D Flatz
Journal:  Humangenetik       Date:  1974

6.  Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation.

Authors:  C Baccichetti; R Tenconi; F Anglani; F Zacchello
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

7.  Partial trisomy 4q: two cases resulting from a familial translocation t(4;18)(q27;p11).

Authors:  A Bonfante; M Stella; G Rossi
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

8.  Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies.

Authors:  R M Lewkonia; C C Lin; R H Haslam
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318
  8 in total

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