Literature DB >> 3879152

Partial monosomy 10p syndrome.

R Koenig, E Kessel, W Schoenberger.   

Abstract

A newborn infant with monosomy 10p13 is reported. The clinical signs and symptoms of the present case are compared with those of previously described cases. Although there is no pathognomonic feature, a characteristic monosomy 10p syndrome is recognizable.

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Mesh：

Year:  1985        PMID： 3879152

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  3 in total

1.  Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism.

Authors:  M M Lai; P N Scriven; C Ball; A C Berry
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features.

Authors:  S A Sanjad; N A Sakati; Y K Abu-Osba; R Kaddoura; R D Milner
Journal:  Arch Dis Child       Date:  1991-02       Impact factor: 3.791

3.  Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.

Authors:  F Greenberg; F F Elder; P Haffner; H Northrup; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025
  3 in total

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