LymphedemaV1, PascalFrancis, Corpus, bibRecord, 001129

Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

Identifieur interne : 001129 ( PascalFrancis/Corpus ); précédent : 001128; suivant : 001130

Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

Auteurs : P. J. Dahlberg ; W. Z. Borer ; K. L. Newcomer ; W. R. Yutuc

Source :

American journal of medical genetics [ 0148-7299 ] ; 1983.

RBID : Pascal:84-0293077

Descripteurs français

Pascal (Inist)
- Lymphoedème, Hypoparathyroïdie, Néphropathie, Prolapsus, Valvule mitrale, Syndrome complexe, Valvulopathie mitrale, Rein pathologie, Cardiopathie, Endocrinopathie, Homme.

English descriptors

KwdEn :
- Complex syndrome, Endocrinopathy, Heart disease, Human, Hypoparathyroidism, Lymphedema, Mitral valve, Mitral valve disease, Nephropathy, Prolapsus, Renal disease.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

A01	`01`	`1`		`@0 0148-7299`
A03		`1`		`@0 Am. j. med. genet.`
A05				`@2 16`
A06				`@2 1`
A08	`01`	`1`	`ENG`	`@1 Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy`
A11	`01`	`1`		`@1 DAHLBERG (P. J.)`
A11	`02`	`1`		`@1 BORER (W. Z.)`
A11	`03`	`1`		`@1 NEWCOMER (K. L.)`
A11	`04`	`1`		`@1 YUTUC (W. R.)`
A14	`01`			`@1 Gundersen Clinic ltd.`
A20				`@1 99-104`
A21				`@1 1983`
A23	`01`			`@0 ENG`
A43	`01`			`@1 CNRS`
A44				`@0 0000`
A45				`@0 8 ref.`
A47	`01`	`1`		`@0 84-0293077`
A60				`@1 P`
A61				`@0 A`
A64		`1`		`@0 American journal of medical genetics`
A66	`01`			`@0 USA`
C02	`01`	`2`		`@0 002B23E`
C03	`01`	`2`	`FRE`	`@0 Lymphoedème`
C03	`02`	`2`	`FRE`	`@0 Hypoparathyroïdie`
C03	`03`	`2`	`FRE`	`@0 Néphropathie`
C03	`04`	`2`	`FRE`	`@0 Prolapsus`
C03	`05`	`2`	`FRE`	`@0 Valvule mitrale`
C03	`06`	`2`	`FRE`	`@0 Syndrome complexe`
C03	`16`	`2`	`FRE`	`@0 Valvulopathie mitrale`
C03	`17`	`2`	`FRE`	`@0 Rein pathologie`
C03	`18`	`2`	`FRE`	`@0 Cardiopathie`
C03	`19`	`2`	`FRE`	`@0 Endocrinopathie`
C03	`20`	`2`	`FRE`	`@0 Homme`
C03	`01`	`2`	`ENG`	`@0 Lymphedema`
C03	`02`	`2`	`ENG`	`@0 Hypoparathyroidism`
C03	`03`	`2`	`ENG`	`@0 Nephropathy`
C03	`04`	`2`	`ENG`	`@0 Prolapsus`
C03	`05`	`2`	`ENG`	`@0 Mitral valve`
C03	`06`	`2`	`ENG`	`@0 Complex syndrome`
C03	`16`	`2`	`ENG`	`@0 Mitral valve disease`
C03	`17`	`2`	`ENG`	`@0 Renal disease`
C03	`18`	`2`	`ENG`	`@0 Heart disease`
C03	`19`	`2`	`ENG`	`@0 Endocrinopathy`
C03	`20`	`2`	`ENG`	`@0 Human`
N21				`@1 340`
N82				`@1 NBS`

Format Inist (serveur)

NO :	PASCAL 84-0293077 INIST
ET :	Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy
AU :	DAHLBERG (P. J.); BORER (W. Z.); NEWCOMER (K. L.); YUTUC (W. R.)
AF :	Gundersen Clinic ltd.
DT :	Publication en série; Niveau analytique
SO :	American journal of medical genetics; ISSN 0148-7299; Etats-Unis; Da. 1983; Vol. 16; No. 1; Pp. 99-104; Bibl. 8 ref.
LA :	Anglais
CC :	002B23E
FD :	Lymphoedème; Hypoparathyroïdie; Néphropathie; Prolapsus; Valvule mitrale; Syndrome complexe; Valvulopathie mitrale; Rein pathologie; Cardiopathie; Endocrinopathie; Homme
ED :	Lymphedema; Hypoparathyroidism; Nephropathy; Prolapsus; Mitral valve; Complex syndrome; Mitral valve disease; Renal disease; Heart disease; Endocrinopathy; Human
LO :	CNRS
ID :	84-0293077

Links to Exploration step

Pascal:84-0293077

Le document en format XML

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<server><NO>PASCAL 84-0293077 INIST</NO>
<ET>Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy</ET>
<AU>DAHLBERG (P. J.); BORER (W. Z.); NEWCOMER (K. L.); YUTUC (W. R.)</AU>
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<LO>CNRS</LO>
<ID>84-0293077</ID>
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Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

Source :

Descripteurs français

English descriptors

Notice en format standard (ISO 2709)

Format Inist (serveur)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri