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Scholar Results 1 - 10 of about 21 citing RATNOFF: The laboratory diagnosis of the carrier state for classic hemophilia. (0.05 sec) 

Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention


H Moser - Human genetics, 1984 - Springer
Summary. Duchenne muscular dystrophy (DMD) is the most common sex linked lethal
disease in man (one case in about 4000 male live births). The patients are
wheelchair bound around the age of 8-10 years and usually die before the ...
Cited by 213 - Related articles - All 3 versions

Duchenne muscular dystrophy


GA Danieli, G Barbujani - Human genetics, 1984 - Springer
Duchenne Muscular Dystrophy (DMD), a well-known genetic lethal in humans, is
transmitted by X-linked recessive in- heritance. The incidence rate for this
disease has been found to be rather high in most human populations; ...
Cited by 42 - Related articles - All 8 versions

[CITATION] Hemostatic disorders of the pregnant woman and newborn infant


WE Hathaway, J Bonnar, 1987 - Elsevier Publishing Company
Cited by 40 - Related articles

Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutation


CT Caskey, RL Nussbaum, LC Cohan, L … - Clin Genet, 1980 - interscience.wiley.com
The mechanism of inheritance of sporadically occurring Duchenne muscular
dystrophy has been investigated in 42 families, using carrier detection methods
and genetic evaluation. Our studies find that serum CPK detects 72 % of ...
Cited by 27 - Related articles - All 3 versions

[CITATION] Factor VIII physiology and pathology in man.


J Koutts, MA Howard, BG Firkin - Progress in hematology, 1979 - ncbi.nlm.nih.gov
1: Prog Hematol. 1979;11:115-45. Factor VIII physiology and pathology in man.
Koutts J, Howard MA, Firkin BG. Publication Types: Review. ...
Cited by 23 - Related articles - All 2 versions

Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis

- leidenuniv.nl [PDF] 
FR Rosendaal, A Bröcker-Vriends, JC … - Human genetics, 1990 - Springer
Summary. A hereditary disease with excess mortality such as haemophilia is
maintained in the population by the occurrence of new cases, ie mutations. In
haemophilia, mutations may arise in female or male ancestors of a 'new' ...
Cited by 22 - Related articles - All 7 versions

Reproduction in hemophilia


RB Francis Jr, CK Kasper - Obstetrical & Gynecological Survey, 1984 - journals.lww.com
Fertility and Family 455 (In the evaluation of infertility, the postcoital test
is a useful test of performance. First, it provides evidence that antegrade
ejaculation actually occurred. Second, abundant mucus gives some indication ...
Cited by 16 - Related articles - All 5 versions

Estimation of male to female ratio of mutation rates from carrier-detection tests in X-linked …

- nih.gov [PDF] 
RM Winter - American Journal of Human Genetics, 1980 - pubmedcentral.nih.gov
SUMMARY A method is presented for the estimation of the ratio of male to female
mutation rates from female carrier-detection test data from pedigrees containing
an isolated male manifesting an X-linked recessive disorder. Pedigrees of ...
Cited by 15 - Related articles - All 3 versions

RFLP analysis in families with sporadic hemophilia A


F Bernardi, G Marchetti, V Bertagnolo, L … - Human genetics, 1987 - Springer
1Centro di Studi Biochimici sul Morbo di Cooley, Universit~ di Ferrara, Via
Luigi Borsari 46, 1-44100 Ferrara, Italy 2Centro per lo Studio e la Terapia
dell'Emofilia, Universit~ di Pisa, 1-56100 Pisa, Italy
Cited by 14 - Related articles - All 3 versions

[CITATION] Clinical aspects of the hemophiliacs and their treatment


CD Forbes - Disorders of Hemostasis. New York, 1984
Cited by 14 - Related articles


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