M. H. K. Shokeir - Concepedia

Author

M. H. K. Shokeir

Also Known As

M H Shokeir, M SHOKEIR, M Shokeir, M. H. K. Shokeir, M. Shokeir, M. Shokeir ., M.H.K Shokeir, M.H.K. Shokeir, Mohamed H Shokeir, Mohamed Shokeir

Publications

1.9K

Citations

H-Index

127

Concepts

All Affiliations

University of Saskatchewan University of Manitoba Royal University Hospital University of Michigan Health Sciences Centre

About

M. H. K. Shokeir is an author at University of Saskatchewan specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	26	833
2	Public Health	5	5	214
3	Health Sciences	3	3	87
4	Natural Sciences	1	1	46
5	Social Sciences	1	1	366

M. H. K. Shokeir

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
PRIMARY SEX-RATIO AND SIZE OF FAMILY M. H. K. Shokeir The Lancet Gender IdentityGender StudiesSex DifferencesSex DifferenceFamily Formation	1970	366
Syndrome of camptodactyly, multiple ankyloses, facial anomalies, and pulmonary hypoplasia: A lethal condition Sérgio D.J. Pena, M. H. K. Shokeir The Journal of Pediatrics Facial AnomaliesPathologyMultiple AnkylosesPulmonary Hypoplasia	1974	205
Autosomal recessive Cerebro‐Oculo‐Facio‐Skeletal (COFS) syndrome Sérgio D.J. Pena, M. H. K. Shokeir Clinical Genetics PathologyAnatomyOsteoporosisOrthopaedic SurgeryClinical Genetics	1974	124
Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment. Shelin Adam, S Wiggins, P Whyte, Journal of Medical Genetics Reproductive HealthGenetic EpidemiologyYear StudyAdult Predictive TestingHigh-risk Pregnancy	1993	109
Dystrophin in frameshift deletion patients with Becker muscular dystrophy. Suman B. Gangopadhyay, T G Sherratt, J Z Heckmatt, PubMed	1992	76
Investigation on Huntington's disease in the Canadian Prairies M. H. K. Shokeir Clinical Genetics	1975	61
Autosomal recessive muscular dystrophy in Manitoba Hutterites* M. H. K. Shokeir, Nathan L. Kobrinsky Clinical Genetics Rare DiseasesMendelian DisorderGenetic DisorderGeneticsFounding Colony	1976	58
Expression of “adult” polycystic renal disease in the fetus and newborn M. H. K. Shokeir Clinical Genetics	1978	55
CYTOCHROME OXIDASE DEFICIENCY IN WILSON'S DISEASE: A SUGGESTED CERULOPLASMIN FUNCTION M. H. K. Shokeir, Donald C. Shreffler Proceedings of the National Academy of Sciences Molecular BiologyPathologyRedox BiologyOxidative StressBioanalysis	1969	46
Aplasia of the Müllerian system: evidence for probable sex-limited autosomal dominant inheritance. M. H. K. Shokeir PubMed Xx IndividualsGeneticsPathologyGynecologyFemale Reproductive System	1978	42

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