Literature DB >> 5519606

Deletion of short arm of no. 4 (4p-)--a detailed case report.

A R Wilcock, F G Adams, P Cooke, R R Gordon.   

Abstract

Mesh：

Year:  1970        PMID： 5519606      PMCID： PMC1468823          DOI： 10.1136/jmg.7.2.171

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  9 in total

1.  [PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].

Authors:  J LEJEUNE; J LAFOURCADE; J DE GROUCHY; R BERGER; M GAUTIER; C SALMON; R TURPIN
Journal:  Sem Hop       Date:  1964-04-14

2.  CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.

Authors:  J GERMAN; J LEJEUNE; M N MACINTYRE; J DE GROUCHY
Journal:  Cytogenetics       Date:  1964

3.  Turner's infantile phenotype.

Authors:  R R Gordon; E M O'Neill
Journal:  Br Med J       Date:  1969-02-22

4.  Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms.

Authors:  D Warburton; D A Miller; O J Miller; W R Breg; A De Capoa; M W Shaw
Journal:  Am J Hum Genet       Date:  1967-05       Impact factor: 11.025

5.  Deletion of short arms of chromosome 4-5 in a child with defects of midline fusion.

Authors:  K Hirschhorn; H L Cooper; I L Firschein
Journal:  Humangenetik       Date:  1965

6.  [Deficiency on the short arms of a chromosome No. 4].

Authors:  U Wolf; H Reinwein; R Porsch; R Schröter; H Baitsch
Journal:  Humangenetik       Date:  1965

7.  [On a case of "crying cat" syndrome with peculiar phenotypic anomalies].

Authors:  P L Giorgi; M Ceccarelli; A Paci
Journal:  Minerva Pediatr       Date:  1965-12-15       Impact factor: 1.312

8.  Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome.

Authors:  O J Miller; W R Breg; D Warburton; D A Miller; I L Firschein; K Hirschhorn
Journal:  Cytogenetics       Date:  1966

9.  New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies.

Authors:  J C Leão; G J Bargman; R L Neu; T Kajii; L I Gardner
Journal:  JAMA       Date:  1967-10-30       Impact factor: 56.272
  9 in total
  7 in total

Review 1.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

2.  The 4p-syndrome, with a report of two new cases.

Authors:  J P Fryns; E Eggermont; H Verresen; H Van den Berghe
Journal:  Humangenetik       Date:  1973

3.  A 4p-syndrome. A case report.

Authors:  A V Mikelsaar; G J Lazjuk; J W Lurie; S Tüür; M E Käosaar; R Mikelsaar; V E Loolaid
Journal:  Humangenetik       Date:  1973-09-20

4.  Pattern analysis of long arm grain count as a criterion of homology in eight cases of Bp.

Authors:  P Cooke; D Headey
Journal:  Humangenetik       Date:  1970-09-17

Review 5.  Toward the complete genomic map and molecular pathology of human chromosome 4.

Authors:  O Riess; B Winkelmann; J T Epplen
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

6.  Neuropathological findings in Wolf-Hirschhorn (4p-) syndrome.

Authors:  M Gottfried; L Lavine; U Roessmann
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

7.  Renal function studies in an infant with 4p (-) syndrome.

Authors:  M Schoeneman; M M Nitowsky
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318
  7 in total

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