Literature DB >> 5410297

C-group chromosome abnormality (? 10p-). Occurrence in a child with multiple malformations.

D Elliott, G H Thomas, C J Condron, N Khuri, F Richardson.   

Abstract

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Year:  1970        PMID: 5410297     DOI: 10.1001/archpedi.1970.02100050074017

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


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  9 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.  MRI findings in a patient with partial monosomy 10p.

Authors:  F Sunada; F C Rash; D A Tam
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

Review 3.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

4.  Partial monosomy 10p syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; F M Alkema
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

5.  Short stature and microgenitalia in the 9p-syndrome.

Authors:  H P Monaghan; N J Howard
Journal:  Ir J Med Sci       Date:  1981-12       Impact factor: 1.568

6.  Two chromosomal syndromes in the same family: monosomy and trisomy for part of the short arm of chromosome 10.

Authors:  S Slinde; I L Hansteen
Journal:  Eur J Pediatr       Date:  1982-10       Impact factor: 3.183

7.  Partial monosomy of chromosome 10 short arms.

Authors:  A Gencík; U Brönniman; R Tobler; P Auf der Maur
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

8.  The 9p-syndrome.

Authors:  S J Funderburk; R S Sparkes; I Klisak
Journal:  J Med Genet       Date:  1979-02       Impact factor: 6.318

9.  Clinical description of a neonate carrying the largest reported deletion involving the 10p15.3p13 region.

Authors:  Saet Byeol Kim; Young-Eun Kim; Ji Mi Jung; Hye Young Jin; Yun-Jung Lim; Mi Lim Chung
Journal:  Clin Case Rep       Date:  2017-07-11
  9 in total

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