Literature DB >> 5365580

Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype.

H Hoehn, W Engel.   

Abstract

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Year:  1969        PMID： 5365580     DOI： 10.1007/bf00295833

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


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  17 in total

1.  CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.

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

2.  "CRI DU CHAT" SYNDROME. A NEW CLINICAL AND CYTOGENETIC ENTITY.

Authors:  J S MCCRACKEN; R R GORDON
Journal:  Lancet       Date:  1965-01-02       Impact factor: 79.321

Review 3.  Autosomal imbalance and its syndromes, excluding down's.

Authors:  P E Polani
Journal:  Br Med Bull       Date:  1969-01       Impact factor: 4.291

4.  [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].

Authors:  S Gilgenkrantz; C Marchal; N Neimann
Journal:  Ann Genet       Date:  1968-03

5.  [New documents of delineation of a syndrome of the deletion of the short arm of one chromosome no 4].

Authors:  R A Pfeiffer
Journal:  Z Kinderheilkd       Date:  1968

6.  Clusterine in deleted short-arm length among 25 cases with a Bp-chromosome.

Authors:  D A Miller; D Warburton; O J Miller
Journal:  Cytogenetics       Date:  1969

Review 7.  The cri-du-chat syndrome with an apparently normal karyotype.

Authors:  D D McGavin; J S Cant; M A Ferguson-Smith; P M Ellis
Journal:  Lancet       Date:  1967-08-12       Impact factor: 79.321

8.  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

9.  Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome.

Authors:  J H Turner; L W Bass; S Kaplan
Journal:  J Med Genet       Date:  1966-03       Impact factor: 6.318

10.  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
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  3 in total

1.  Human chromosomal deficiency: the 4p--syndrome.

Authors:  E Passarge; H C Altrogge; R A Rüdiger
Journal:  Humangenetik       Date:  1970-08-17

2.  The 18 p-syndrome. Report of four cases.

Authors:  J Faust; M Habedank; C Nieuwenhuijsen
Journal:  Eur J Pediatr       Date:  1976-08-16       Impact factor: 3.183

Review 3.  The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors:  E Niebuhr
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132
  3 in total

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