Literature DB >> 5862078

Carrier detection in sex-linked muscular dystrophy.

A E Emery.   

Abstract

Mesh：

Substances：

Year:  1965        PMID： 5862078

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


× No keyword cloud information.
  11 in total

1.  The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.

Authors:  R Skinner; A E Emery; A J Anderson; C Foxall
Journal:  J Med Genet       Date:  1975-06       Impact factor: 6.318

2.  [Creatine phosphokinase activity in serum of carriers of progressive muscular dystrophy of Duchenne type].

Authors:  W Barthelmai; G Dikbas; S Wüllner
Journal:  Humangenetik       Date:  1969-10

3.  [Diagnosis of female carriers of Duchenne's progressive muscular dystrophy using discriminative analysis of various serum enzyme activities].

Authors:  C M Büsing; H Heyck; G Laudahn
Journal:  Klin Wochenschr       Date:  1969-10-15

4.  [Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].

Authors:  H Moser
Journal:  Humangenetik       Date:  1971

5.  [Serum creatine kinase and sulphydryl concentration after ischemic forearm work in patients and carriers of Duchenne's progressive muscular dystrophy].

Authors:  H Moser; U Wiesmann
Journal:  Klin Wochenschr       Date:  1971-04-15

6.  A simple method for calculating risks before DNA analysis.

Authors:  M Jeanpierre
Journal:  J Med Genet       Date:  1988-10       Impact factor: 6.318

7.  LDH isozyme pattern in induced muscle disease (Coxsackie Group A virus infection).

Authors:  S Kelly; A Belorit
Journal:  Experientia       Date:  1967-07-15

8.  The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.

Authors:  A J van Essen; A L Kneppers; A H van der Hout; H Scheffer; I B Ginjaar; L P ten Kate; G J van Ommen; C H Buys; E Bakker
Journal:  J Med Genet       Date:  1997-10       Impact factor: 6.318

9.  Histochemically demonstrable fibre abnormalities in normal skeletal muscle and in muscle from carriers of Duchenne muscular dystrophy.

Authors:  C J Morris; J A Raybould
Journal:  J Neurol Neurosurg Psychiatry       Date:  1971-06       Impact factor: 10.154

10.  Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Authors:  M Lindlöf; H Kääriäinen; K E Davies; A de la Chapelle
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.