Literature DB >> 1150249

Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).

C Stoll, J M Levy, A Gardea.   

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Year:  1975        PMID: 1150249     DOI: 10.1007/bf00278358

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


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  7 in total

1.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Authors:  M O Rethoré; H Hoehn; H D Rott; J Couturier; B Dutrillaux; J Lejeune
Journal:  Humangenetik       Date:  1973-04-16

2.  [A new technic of analysis of the human karyotype].

Authors:  B Dutrillaux; J Lejeune
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1971-05-17

3.  Trisomy 9 mosaicism with multiple congenital anomalies.

Authors:  R H Haslam; S P Broske; C M Moore; G H Thomas; C A Neill
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

4.  A case of trisomy 9.

Authors:  M Feingold; L Atkins
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

5.  Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.

Authors:  A J Ebbin; M G Wilson; J W Towner; J P Slaughter
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

6.  [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].

Authors:  M O Rethoré; L Larget-Piet; D Abonyi; M Boeswillwald; R Berger; S Carpentier; J Cruveiller; B Dutrillau; J Lafourcade; M Penneau; J Lejeune
Journal:  Ann Genet       Date:  1970-12

7.  Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Authors:  H Hoehn; W Engel; H Reinwein
Journal:  Humangenetik       Date:  1971
  7 in total
  11 in total

1.  Possible intrachromosomal duplication in a case of trisomy 9p.

Authors:  H Chiyo; J Furuyama; N Suehara; Y Obashi; H Kikkawa
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

2.  Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975-12-23

3.  47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

Authors:  H Fujita; M Shimazaki; T Takeuchi; Y Hayakawa; T Oura
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

4.  De novo trisomy 9pter leads to q13.

Authors:  N B Kardon; H R Salwen; M A Krauss; J G Davis; E C Jenkins
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

Review 5.  Genetics of the +p9 syndrome.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

6.  Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

Authors:  M Tolksdorf; J Kunze; G Gross-Selbeck; K Sperling; R D Wegner; V Wieczorek; M Vogel
Journal:  Eur J Pediatr       Date:  1977-08-23       Impact factor: 3.183

7.  Sister chromatid exchanges in balanced translocation carriers and in patients with unbalanced karyotypes.

Authors:  C Stoll; D S Borgaonkar; P Bigel
Journal:  Hum Genet       Date:  1977-06-10       Impact factor: 4.132

Review 8.  Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors:  P Jalbert; B Sele
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

9.  Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Authors:  P Jalbert; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

10.  Nonrandom distribution of exchange points in patients with reciprocal translocations.

Authors:  C Stoll
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

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