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MENDELIAN GENETICS I
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card_57381.txt
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1989-06-13
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1KB
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65 lines
-- card: 57381 from stack: in
-- bmap block id: 60974
-- flags: 0000
-- background id: 2665
-- name:
-- part 1 (button)
-- low flags: 00
-- high flags: 8003
-- rect: left=157 top=315 right=337 bottom=257
-- title width / last selected line: 0
-- icon id / first selected line: 0 / 0
-- text alignment: 1
-- font id: 0
-- text size: 12
-- style flags: 0
-- line height: 16
-- part name: SUB HEADINGS
----- HyperTalk script -----
on mouseUp
go to card id 58743
end mouseUp
-- part contents for background part 1
----- text -----
HUMAN GENETIC DISORDERS
-- part contents for background part 2
----- text -----
alkaptonuria (darkening of urine)
retardation
phenylketonuria
Lesch-Nihan Syndrome
cri du chat
infantile amaurotic idiocy
Tay-Sachs disease
vitamin D-resistant rickets
Hutchinson-Gilford syndrome
Premature ageing
Duchenne's syndrome
Muscular dystrophy
Allport's syndrome
deafness, hemoglobin in urine
juvenile amaurotic idiocy
Rotor syndrome
(mild jaundice)
pattern baldness
polycystic kidney disease
gout
diabetes mellitus
Alzheimer's disease
Huntington's chorea
Turner's syndrome
XO female
Klienfelter's syndrome
XXY male
-- part contents for background part 8
----- text -----
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