42:
98:. They may give editors a more specific focus on the aspects of medical genetics. They are merely intended as a guide, not as a preset way of writing. All are open to debate, if you wish to add or edit these advice, please do so or discuss your suggestions
99:
183:
in newspapers, fundraising materials, or personal blogs. At the same time, external links should help families and individuals find outside sources that are up-to-date and accurate, yet accessible to non-technical readers.
192:
If an article relates to a particular chromosome the specific chromosome number should be linked to, and also consider whether the chromosome page would benefit from mentioning the article.
21:
87:
208:
316:
352:
218:
66:
347:
71:
171:
It is important that information about causes, detection, treatment, and so forth reference high-quality medical textbooks and
17:
213:
144:
Articles should respect the feelings of readers who may have a genetic condition: some may not like the use of the word
204:
may be used for some articles worked on by this project, but also look for other categories and subcategories such as:
283:
201:
75:
54:
27:
180:
254:
inheritance of genetic disorders can be depicted with an explanatory diagram on each page, for example:
60:
320:
114:
324:
125:
311:
133:
50:
264:
inheritance of genetic disorders can be depicted with an equivalent diagram on each page:
234:
176:
341:
91:
86:
The following suggestions are in addition to the guidelines for medical articles at
95:
307:
172:
160:
119:
63:
on how to format and present article content within their area of interest.
289:
241:{{WPMED |class=stub |importance= |genetics=yes |genetics-imp= }}
41:
331:
302:
159:
A good article on which phrases are preferred can be found at
36:
281:
Some images used to depict genetic inheritance are in the
229:
Stubs relating to medical genetics can be tagged with the
330:
Source of molecule images that seems to be public domain
237:
template by inserting this into the article's talk page.
88:
Knowledge:Manual of Style (medicine-related articles)
59:It contains the advice or opinions of one or more
28:Knowledge:WikiProject Medical Genetics/Guidelines
8:
209:Category:Chromosome instability syndromes
161:http://www.apastyle.org/disabilities.html
274:(including dominant and recessive) and
179:, rather than low-quality sources like
90:, as well as the general guidelines at
317:Merck Manual of Diagnosis and Therapy
7:
219:Category:Inborn errors of metabolism
312:Medical Encyclopedia on Medlineplus
290:Wikimedia commons genetics category
76:thoroughly vetted by the community
35:
284:Medical genetics images category
92:Guide to writing better articles
40:
233:template. Remember to add the
18:Knowledge:WikiProject Medicine
1:
214:Category:Congenital disorders
72:Knowledge policy or guideline
332:http://www.rcsb.org/pdb/home
297:Reliable sources, references
353:Medical genetics task force
22:Medical genetics task force
369:
270:There are also images for
202:genetic disorders category
327:can be used in articles).
231:{{genetic-disorder-stub}}
348:WikiProject style advice
106:The scope of the project
181:human-interest stories
110:The project works on:
152:. Use words such as
74:, as it has not been
175:studies, especially
115:congenital disorders
96:Article development
136:related articles.
120:monogenic disorder
84:
83:
26:(Redirected from
360:
321:The Merck Manual
287:. Others are on
188:Chromosome links
134:medical genetics
70:is not a formal
67:This information
44:
37:
31:
368:
367:
363:
362:
361:
359:
358:
357:
338:
337:
303:geneclinics.org
299:
268:
258:
248:
227:
198:
190:
177:review articles
169:
167:Source material
142:
108:
80:
79:
33:
32:
25:
24:
12:
11:
5:
366:
364:
356:
355:
350:
340:
339:
336:
335:
328:
323:(the template
314:
305:
298:
295:
266:
256:
247:
244:
243:
242:
226:
223:
222:
221:
216:
211:
197:
194:
189:
186:
168:
165:
141:
138:
130:
129:
123:
117:
107:
104:
82:
81:
64:
47:
45:
34:
15:
14:
13:
10:
9:
6:
4:
3:
2:
365:
354:
351:
349:
346:
345:
343:
333:
329:
326:
322:
318:
315:
313:
309:
306:
304:
301:
300:
296:
294:
292:
291:
286:
285:
279:
277:
273:
265:
263:
255:
253:
245:
240:
239:
238:
236:
232:
224:
220:
217:
215:
212:
210:
207:
206:
205:
203:
195:
193:
187:
185:
182:
178:
174:
173:peer-reviewed
166:
164:
162:
157:
155:
151:
147:
139:
137:
135:
132:Mainly every
127:
124:
122:(single gene)
121:
118:
116:
113:
112:
111:
105:
103:
101:
97:
93:
89:
77:
73:
69:
68:
62:
58:
56:
52:
46:
43:
39:
38:
29:
23:
19:
288:
282:
280:
275:
271:
269:
261:
259:
251:
249:
230:
228:
199:
191:
170:
158:
153:
149:
145:
143:
131:
109:
85:
65:
61:WikiProjects
48:
308:MedlinePlus
276:co-dominant
156:carefully.
140:Sensitivity
49:This is an
342:Categories
196:Categories
325:MerckHome
319:website:
252:recessive
128:disorders
126:polygenic
272:X-linked
262:dominant
154:mutation
150:disorder
20: |
146:disease
246:Images
235:WPMED
225:Stubs
55:style
51:essay
16:<
260:The
250:The
200:The
100:here
94:and
148:or
53:on
344::
310:-
293:.
278:.
267:]
257:]
163:.
102:.
334:.
78:.
57:.
30:)
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
