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X-linked recessive inheritance scenarios for either the mother being a carrier or the father being affected
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358:– If you remix, transform, or build upon the material, you must distribute your contributions under the
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For use on syndromes in which an affected male might be expected to pass on the condition. If not, use
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Keratosis follicularis-dwarfism-cerebral atrophy syndrome
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Creative
Commons Attribution-ShareAlike 4.0 International
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Hypohidrotic ectodermal dysplasia with immune deficiency
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Add a one-line explanation of what this file represents
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Commons is a freely licensed media file repository.
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Pierre Robin sequence-faciodigital anomaly syndrome
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Switched carrier mother children to be more centred
863:Biologia per il liceo/La genetica post-mendeliana
730:X-linked complicated corpus callosum dysgenesis
369:https://creativecommons.org/licenses/by-sa/4.0
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375:Creative Commons Attribution-Share Alike 4.0
299:
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335:– to copy, distribute and transmit the work
46:Size of this PNG preview of this SVG file:
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770:The following other wikis use this file:
750:X-linked severe combined immunodeficiency
322:Attribution-Share Alike 4.0 International
257:X-linked recessive (affected father).svg
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230:X-linked recessive (carrier mother).svg
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665:The following 19 pages use this file:
740:X-linked recessive hypoparathyroidism
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848:Atrofia muscolare spinale e bulbare
655:User created page with UploadWizard
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853:Ereditarietà legata al cromosoma X
715:Spinal and bulbar muscular atrophy
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186:File:Autosomal recessive - en.svg
174:File:Autosomal recessive - en.svg
793:X-vezano recesivno nasljeđivanje
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317:This file is licensed under the
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745:X-linked recessive inheritance
725:Tranebjaerg–Svejgaard syndrome
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412:Items portrayed in this file
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889:Usage on zh.wikipedia.org
879:Usage on sr.wikipedia.org
869:Usage on ja.wikipedia.org
859:Usage on it.wikibooks.org
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834:Usage on id.wikipedia.org
824:Usage on he.wikipedia.org
814:Usage on ga.wikipedia.org
799:Usage on el.wikipedia.org
789:Usage on bs.wikipedia.org
774:Usage on ar.wikipedia.org
720:Stocco dos Santos syndrome
360:same or compatible license
143:X-linked recessive (2).svg
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783:متلازمة ستوكو دوس سانتوس
735:X-linked genetic disease
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104:This is a file from the
808:Μυϊκή δυστροφία Ντουσέν
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111:description page there
828:תאחיזה לכרומוזומי מין
760:User talk:Ozzie10aaaa
74:1,525 × 1,283 pixels
70:2,434 × 2,048 pixels
66:1,217 × 1,024 pixels
341:– to adapt the work
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670:Gustavson syndrome
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778:متلازمة غوستافسون
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710:Rud syndrome
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571:File history
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119:You can help
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22:File history
838:Hemofilia B
818:Haemaifilia
675:Haemophilia
450:copyrighted
356:share alike
350:attribution
141:Description
661:File usage
588:Dimensions
540:media type
27:File usage
925:1283.3542
585:Thumbnail
582:Date/Time
506:inception
293:Licensing
242:InfoField
214:InfoField
150:English:
901:Metadata
644:(170 KB)
614:(169 KB)
393:Captions
339:to remix
333:to share
324:license.
235:instead.
194:Kashmiri
37:Metadata
893:X連鎖隱性遺傳
599:current
594:Comment
417:depicts
397:English
282:español
270:العربية
190:Domaina
133:Summary
85:
922:Height
180:Author
169:Source
914:Width
917:1525
873:血友病B
650:SUM1
620:SUM1
591:User
381:true
378:true
212:Note
204:SUM1
198:SUM1
196:and
159:Date
17:File
192:,
188::
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Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
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