SCOPUS 정보 검색 플랫폼

Volumn 4, Issue 12, 1997, Pages 1264-1265

Atrésie jejunale et syndrome de persistance des dérivés miillériens

(9) Klosowski, S a Abriak, A a Morisot, C a Bayart, H C a Belville, C a Thelliez, P b Gottrand, F b Croquette, M F c Deroubaix, P d

a Centre Hospitalier de LENS (France)

b ECOLE NORMALE SUPÉRIEURE (France)

c Hôpital Jeanne deFlandre (France)

d HÔPITAL SAINT ANTOINE (France)

Author keywords

[No Author keywords available]

Indexed keywords

TESTIS PEPTIDE HORMONE;

CASE REPORT; CONGENITAL MALFORMATION; HUMAN; INTESTINE ATRESIA; JEJUNUM; LETTER; MALE; MUELLERIAN DUCT; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PHYSIOLOGY; TESTIS;

ABNORMALITIES, MULTIPLE; HUMANS; INFANT, NEWBORN; INTESTINAL ATRESIA; JEJUNUM; MALE; MULLERIAN DUCTS; TESTICULAR HORMONES; TESTIS;

EID: 0031300857 PISSN: 0929693X EISSN: None Source Type: Journal
DOI: 10.1016/S0929-693X(97)82624-3 Document Type: Article

Times cited : (6)

References (7)

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- Loeff, D.S.¹ Imbeaud, S.² Reyes, H.M.³ Melier, J.L.⁴ Rosenthal, I.M.⁵

2
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- Le syndrome de persistance des dérivés mullériens (hommes à utérus) : Un problème pédiatrique
- Zeller J, Imbeaud S, Rey R et al. Le syndrome de persistance des dérivés mullériens (hommes à utérus) : un problème pédiatrique. Arch Pediatr 1994; 1: 991-7
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- Zeller, J.¹ Imbeaud, S.² Rey, R.³

3
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- Les atrésies jéjuno-iléales
- Gruner M, Chaouachi B, Goutet JM, Navarro J. Les atrésies jéjuno-iléales. Rev Prat 1981;31:1191-1205
- (1981) Rev Prat , vol.31 , pp. 1191-1205
- Gruner, M.¹ Chaouachi, B.² Goutet, J.M.³ Navarro, J.⁴

4
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- L'hormone anti-miillérienne en clinique humaine
- Josso N, Rey R. L'hormone anti-miillérienne en clinique humaine. Contracept Fenil Sex 1994;22:661-3
- (1994) Contracept Fenil Sex , vol.22 , pp. 661-663
- Josso, N.¹ Rey, R.²

5
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- Mapping of the gene for anti-Müllerian hormone to the short arm of human chromosome 19
- Cohen-Haguenauer O, Picard JY, Mattéi MG et al. Mapping of the gene for anti-Müllerian hormone to the short arm of human chromosome 19. Cytogenet Cell Genet 1987; 44:2-6
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- Cohen-Haguenauer, O.¹ Picard, J.Y.² Mattéi, M.G.³

6
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- Insensitivity to antiMullerian hormone due to a mutation in the human antiMullerian hormone receptor
- Imbeaud S, Faure E, Lamarre I et al. Insensitivity to antiMullerian hormone due to a mutation in the human antiMullerian hormone receptor. Nature Genet 1995;11: 382-8
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7
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- A 27 base-pair deletion of the anti-Miillerian type II receptor gene is the most common cause of the persistent milllerian duct syndrome
- Imbeaud S, Belville C, Messika-Zeitoun L et al. A 27 base-pair deletion of the anti-Miillerian type II receptor gene is the most common cause of the persistent milllerian duct syndrome. Hum Mol Genet 1996;5:1269-77
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.