نتایج جستجو برای: dermatoglyphic

تعداد نتایج: 372  

Journal: :Circulation 1970
M Alter R Schulenberg

SUMMARY Dermatoglyphics form in utero during early gestation and may be influenced by genetic or environmental factors operating at that time. Since cardiac embryogenesis also occurs during early gestation, an analysis of dermatoglyphics in congenital heart disease (CHD) miight reveal some types which are associated with aberrant dermato-glyphics. Ten dermatoglyphic traits were analyzed in 225 ...

2005
RICHARD C. JUBERG DALAND R. JUBERG

In investigating the dermatoglyphics of hyperactive subjects, it was proposed that if similar hyperactives were sampled and significant differences were found from suitable controls, a genetic effect could be responsible. From two clinical populations, we ascertained 26 subjects in 24 sibships comprising the hyperactive study group. The control subjects came from an earlier study. Tables 2-9 co...

Journal: :Journal of medical genetics 1980
M Holmes-Siedle S Kerr R H Lindenbaum M Bobrow

Parents of patients with Down's syndrome show dermatoglyphic features intermediate between the affected and the normal population. Dermatoglyphs were studied on the parents of 19 cases of trisomy 18, but no similar "intermediate" traits were discovered. The number of cases studied needs to be enlarged before it can definitely be stated that trisomies 18 and 21 differ in this respect.

2016
Buddhika T B Wijerathne Robert J Meier Suneth B Agampodi

INTRODUCTION Tel Hashomer camptodactyly syndrome is a rare disease and only a few cases have been reported. Dermatoglyphics potentially provide relevant phenotypic biomarkers that were initially noted as a vital clinical feature of this disease. Dermatoglyphics possibly can indicate growth disturbances that took place during early fetal development at the time when epidermal ridges were being f...

Journal: :Journal of medical genetics 1977
C G Palmer M E Hodes T Reed J Kojetin

Four new cases of ring G chromosomes are presented including one family in which the ring 21 is present in a mother and in her daughter, who has 47, XXX, r(21) chromosomes. The clinical and dermatoglyphic findings in r21 and r22 syndromes are reviewed.

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