Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly
| Medienart: |
E-Artikel |
|---|
| Erscheinungsjahr: |
2017 |
|---|---|
| Erschienen: |
2017 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:92 |
|---|---|
| Enthalten in: |
Clinical genetics - 92(2017), 5 vom: 31. Nov., Seite 556-558 |
| Sprache: |
Englisch |
|---|
| Beteiligte Personen: |
Lavillaureix, A [VerfasserIn] |
|---|
| Links: |
|---|
| Themen: |
|---|
| Anmerkungen: |
Date Completed 18.03.2019 Date Revised 18.03.2019 published: Print-Electronic Citation Status MEDLINE |
|---|
| doi: |
10.1111/cge.13062 |
|---|
| funding: |
|
|---|---|
| Förderinstitution / Projekttitel: |
|
| PPN (Katalog-ID): |
NLM274367793 |
|---|
| LEADER | 01000naa a22002652 4500 | ||
|---|---|---|---|
| 001 | NLM274367793 | ||
| 003 | DE-627 | ||
| 005 | 20231225003330.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 231225s2017 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1111/cge.13062 |2 doi | |
| 028 | 5 | 2 | |a pubmed24n0914.xml |
| 035 | |a (DE-627)NLM274367793 | ||
| 035 | |a (NLM)28762477 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 100 | 1 | |a Lavillaureix, A |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly |
| 264 | 1 | |c 2017 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ƒaComputermedien |b c |2 rdamedia | ||
| 338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a Date Completed 18.03.2019 | ||
| 500 | |a Date Revised 18.03.2019 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 650 | 4 | |a Letter | |
| 650 | 7 | |a FBN2 protein, human |2 NLM | |
| 650 | 7 | |a Fibrillin-2 |2 NLM | |
| 700 | 1 | |a Heide, S |e verfasserin |4 aut | |
| 700 | 1 | |a Chantot-Bastaraud, S |e verfasserin |4 aut | |
| 700 | 1 | |a Marey, I |e verfasserin |4 aut | |
| 700 | 1 | |a Keren, B |e verfasserin |4 aut | |
| 700 | 1 | |a Grigorescu, R |e verfasserin |4 aut | |
| 700 | 1 | |a Jouannic, J M |e verfasserin |4 aut | |
| 700 | 1 | |a Gelot, A |e verfasserin |4 aut | |
| 700 | 1 | |a Whalen, S |e verfasserin |4 aut | |
| 700 | 1 | |a Héron, D |e verfasserin |4 aut | |
| 700 | 1 | |a Siffroi, J P |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Clinical genetics |d 1971 |g 92(2017), 5 vom: 31. Nov., Seite 556-558 |w (DE-627)NLM00004914X |x 1399-0004 |7 nnns |
| 773 | 1 | 8 | |g volume:92 |g year:2017 |g number:5 |g day:31 |g month:11 |g pages:556-558 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.1111/cge.13062 |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a GBV_NLM | ||
| 951 | |a AR | ||
| 952 | |d 92 |j 2017 |e 5 |b 31 |c 11 |h 556-558 | ||