36 related articles for article (PubMed ID: 11802385)
1. Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease.
Janssens K; Gershoni-Baruch R; GuaƱabens N; Migone N; Ralston S; Bonduelle M; Lissens W; Van Maldergem L; Vanhoenacker F; Verbruggen L; Van Hul W
Nat Genet; 2000 Nov; 26(3):273-5. PubMed ID: 11062463
[TBL] [Abstract][Full Text] [Related]
2. Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease.
Kinoshita A; Saito T; Tomita H; Makita Y; Yoshida K; Ghadami M; Yamada K; Kondo S; Ikegawa S; Nishimura G; Fukushima Y; Nakagomi T; Saito H; Sugimoto T; Kamegaya M; Hisa K; Murray JC; Taniguchi N; Niikawa N; Yoshiura K
Nat Genet; 2000 Sep; 26(1):19-20. PubMed ID: 10973241
[TBL] [Abstract][Full Text] [Related]
3. Preaxial polydactyly in the 4p- syndrome.
Schrander-Stumpel CT; Rijnvos WP; van der Blij-Philipsen M; Drogtrop A; Smeets D; Fryns JP
Genet Couns; 1998; 9(1):63-5. PubMed ID: 9555593
[No Abstract] [Full Text] [Related]
4. Pallister-Hall syndrome.
Olney AH; Kolodziej P
Ear Nose Throat J; 1998 May; 77(5):370. PubMed ID: 9615516
[No Abstract] [Full Text] [Related]
5. Domain-specific mutations of a transforming growth factor (TGF)-beta 1 latency-associated peptide cause Camurati-Engelmann disease because of the formation of a constitutively active form of TGF-beta 1.
Saito T; Kinoshita A; Yoshiura Ki ; Makita Y; Wakui K; Honke K; Niikawa N; Taniguchi N
J Biol Chem; 2001 Apr; 276(15):11469-72. PubMed ID: 11278244
[TBL] [Abstract][Full Text] [Related]
6. [Positional cloning of anomaly-syndrome-causing genes].
Niikawa N
Tanpakushitsu Kakusan Koso; 2001 Dec; 46(16 Suppl):2313-8. PubMed ID: 11802385
[No Abstract] [Full Text] [Related]
7. [Greig cephalopolysyndactyly syndrome].
Satokata I
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):184-6. PubMed ID: 11057189
[No Abstract] [Full Text] [Related]
8. Polydactyly: how many disorders and how many genes?
Biesecker LG
Am J Med Genet; 2002 Oct; 112(3):279-83. PubMed ID: 12357471
[TBL] [Abstract][Full Text] [Related]
9. The genetic aetiology of Silver-Russell syndrome.
Abu-Amero S; Monk D; Frost J; Preece M; Stanier P; Moore GE
J Med Genet; 2008 Apr; 45(4):193-9. PubMed ID: 18156438
[TBL] [Abstract][Full Text] [Related]
10. [Camurati-Engelmann disease].
Kinoshita A
Nihon Rinsho; 2015 Dec; 73(12):2149-59. PubMed ID: 26666167
[TBL] [Abstract][Full Text] [Related]
11. Smith-Magenis syndrome.
Elsea SH; Girirajan S
Eur J Hum Genet; 2008 Apr; 16(4):412-21. PubMed ID: 18231123
[TBL] [Abstract][Full Text] [Related]
12. [Camptomelic dysplasia].
Tonoki H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):306-7. PubMed ID: 11057239
[No Abstract] [Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]