Literature DB >> 4844639

Brother and sister with trisomy 10p: a new syndrome.

E Schleiermacher, U Schliebitz, C Steffens.   

Abstract

Mesh：

Year:  1974        PMID： 4844639     DOI： 10.1007/bf00285102

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


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  12 in total

1.  Partial trisomy of 7q resulting from a familial translocation.

Authors:  E Grace; G R Sutherland; G D Stark; A D Bain
Journal:  Ann Genet       Date:  1973-03

2.  [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

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

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

4.  [2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].

Authors:  J de Grouchy; C Finaz; M Roubin; J Roy
Journal:  Ann Genet       Date:  1972-06

5.  A familial translocation t(6q+;8q-) identified by fluorescence microscopy.

Authors:  E Niebuhr
Journal:  Humangenetik       Date:  1973-04-16

6.  C8 trisomy mosaicism syndrome.

Authors:  J B Bijlsma; J C Wijffels; W H Tegelaers
Journal:  Helv Paediatr Acta       Date:  1972-07

7.  [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

8.  [Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].

Authors:  H D Rott; G Schwanitz; K P Grosse
Journal:  Z Kinderheilkd       Date:  1971

9.  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

10.  [Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].

Authors:  C Laurent; M Bovier-Lapierre; B Dutrillaux
Journal:  Humangenetik       Date:  1973
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  18 in total

1.  Del (10)p autosomal deletion syndrome: clinical, cytogenetic and gene marker studies.

Authors:  U Francke; C Kernahan; C Bradshaw
Journal:  Humangenetik       Date:  1975

2.  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

3.  Risk for short arm 10 trisomy. A segregation analysis of eleven families with different translocations.

Authors:  J Stene; S Stengel-Rutkowski
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

4.  New chromosomal dysmorphic syndromes. 2. Trisomy 10p.

Authors:  S Stengel-Rutkowski; J D Murken; R Frankenberger; M Riechert; H Spiess; A Rodewald; J Stene
Journal:  Eur J Pediatr       Date:  1977-10-12       Impact factor: 3.183

5.  Neurophysiological findings in a newborn with chromosome 10 trisomy.

Authors:  Simone Vidale; Franco Di Palma; Luigi Sironi; Marco Arnaboldi
Journal:  BMJ Case Rep       Date:  2014-05-05

6.  Partial duplication of the short arm of chromosome 10. Karyotype: 46,XX,dup(10p)(pter to p12::p12::p12 to qter).

Authors:  J P Fryns; J Deroover; J Haegeman; H Van den Berghe
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

7.  Partial trisomy 10p and familial translocation t(7;10)(p22;p12).

Authors:  G Johnson; R Bachman; T Roed; P Riddervold
Journal:  Hum Genet       Date:  1977-03-14       Impact factor: 4.132

8.  Partial trisomy 10p in two generations.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; G I Kravtzoa; M K Nedzved; I A Shved
Journal:  Hum Genet       Date:  1978-03-17       Impact factor: 4.132

9.  Partial trisomy 10p.

Authors:  K P Grosse; G Schwanitz; H Singer; V Wieczorek
Journal:  Humangenetik       Date:  1975-09-10

10.  Duplication deficiency as the result of meiotic segregation of a maternal InV (10).

Authors:  E Yunis; O Torres de Caballero
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
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