Literature DB >> 5049069

[Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

A Schinzel, W Schmid.   

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Year:  1972        PMID： 5049069     DOI： 10.1007/bf00295743

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


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  16 in total

1.  A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.

Authors:  K H GUSTAVSON; S C FINLEY; W H FINLEY; B JALLING
Journal:  Acta Paediatr       Date:  1964-03       Impact factor: 2.299

2.  [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

Authors:  J LEJEUNE; R BERGER; M O RETHORE; L ARCHAMBAULT; H JEROME; S THIEFFRY; J AICARDI; M BROYER; J LAFOURCADE; J CRUVEILLER; R TURPIN
Journal:  C R Hebd Seances Acad Sci       Date:  1964-11-30

3.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

4.  [Partial deletion of the short arm of chromosome 4 (Wolf's syndrome). Two further cases].

Authors:  A Schinzel; W Schmid
Journal:  Arch Genet (Zur)       Date:  1972

5.  A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation.

Authors:  H Grotsky; L Y Hsu; K Hirschhorn
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

6.  [Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].

Authors:  J Lejeune; R Berger; J Lafourcade; M O Réthoré
Journal:  Ann Genet       Date:  1966

7.  Clinical and chromosomal studies of the 18q- syndrome.

Authors:  W Wertelecki; P S Gerald
Journal:  J Pediatr       Date:  1971-01       Impact factor: 4.406

8.  The cat cry syndrome (5p-) in adolescents and adults.

Authors:  E Niebuhr
Journal:  J Ment Defic Res       Date:  1971-12

9.  Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

Authors:  A De Capoa; D Warburton; W R Breg; D A Miller; O J Miller
Journal:  Am J Hum Genet       Date:  1967-07       Impact factor: 11.025

10.  [Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].

Authors:  C Laurent; J M Robert
Journal:  Ann Genet       Date:  1966-09
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  14 in total

1.  Hand dermatoglyphics in trisomy 4p.

Authors:  P Mastroiacovo; V Currò; A Calabro; B Dallapiccola
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

2.  A case of trisomy of the short arms of chromosome no. 4 with translocation t(4p 21p; 4q 21q) in the mother.

Authors:  M Furbetta; G Rosi; P Cossu; A Cao
Journal:  Humangenetik       Date:  1975

3.  [Trisomy 4p. Three new observations (author's transl)].

Authors:  F Giraud; J F Mattei; M G Mattei; S Ayme; R Bernard
Journal:  Humangenetik       Date:  1975-11-06

4.  The radiological pattern associated with the trisomy of the short arm of chromosome No 4.

Authors:  B Dallapiccola; G Giovannelli; A Forabosco
Journal:  Pediatr Radiol       Date:  1975-01-24

5.  'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.

Authors:  F S Brimblecombe; F J Lewis; M Vowles
Journal:  J Med Genet       Date:  1977-08       Impact factor: 6.318

6.  Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family.

Authors:  M Andrle; A Erlach; W Killian; A Rett
Journal:  Hum Genet       Date:  1976-07-27       Impact factor: 4.132

7.  Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

Authors:  L Owen; B Martin; C E Blank; F Harris
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

8.  [Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].

Authors:  F Metz; L Bier; R A Pfeiffer
Journal:  Humangenetik       Date:  1973-05-25

9.  Structural aberrations of chromosome 18. II. The 18q- syndrome. Report of three cases.

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

10.  Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.

Authors:  H Schröchsnadel; C Feichtinger; C Scheminzky
Journal:  Humangenetik       Date:  1975-10-07
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