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LAURENCE/MOON/BEIDL SYNDROMECUNLIFFE W.1981; BR. ORTHOPT. J.; GBR; DA. 1981; NO 38; PP. 79-81Article

THE POSSIBLE RELATIONSHIP BETWEEN LAURENCE-MOON-BIEDL-BARDET SYNDROME AND A SCHIZOPHRENIC-LIKE PSYCHOSISWEISS M; MESHULAM B; WIJSENBEEK H et al.1981; J. NERV. MENT. DIS.; ISSN 0022-3018; USA; DA. 1981; VOL. 169; NO 4; PP. 259-260; BIBL. 10 REF.Article

THE LAURENCE-MOON-BIEDL SYNDROME. SIX CASES OF OBESITY, SHORT STATURE, MENTAL RETARDATION, SMALL GENITALIA, AND RETINITIS PIGMENTOSA. = LE SYNDROME DE LAURENCE-MOON-BIEDL. SIX CAS D'OBESITE PETITE TAILLE RETARD MENTAL, HYPOPLASIE GENITALE ET RETINITE PIGMENTAIREMOINI AR; EMAMY H; PATH D et al.1975; CLIN. PEDIATR.; U.S.A.; DA. 1975; VOL. 14; NO 9; PP. 812-815; BIBL. 15 REF.Article

LA MALADIE DE LAURENCE-MOON-BARDET-BIEDL. CONTRIBUTION CLINIQUELOVISETTO P; BIARESE V; TRENTA N et al.1974; ANN. ENDOCRINOL.; FR.; DA. 1974; VOL. 35; NO 5; PP. 547-561; ABS. ANGL.; BIBL. 9REF.Article

THE LAURENCE-MOON-BIELD SYNDROME IN A SINGHALESE FAMILY.CHANMUGAM D; FERNANDO RL; KARUNAHARAN T et al.1977; AUSTRAL. NEW ZEAL. J. MED.; AUSTRAL.; DA. 1977; VOL. 7; NO 3; PP. 304-306; BIBL. 15 REF.Article

Retinal function in carriers of Bardet-Biedl syndromeCOX, Gerald F; HANSEN, Ronald M; QUINN, Nicole et al.Archives of ophthalmology (1960). 2003, Vol 121, Num 6, pp 804-810, issn 0003-9950, 7 p.Article

PITUITARY AND GONADAL FUNCTION IN PATIENTS WITH THE LAURENCE-MOON-BIEDL SYNDROME.PEREZ PALACIOS G; URIBE M; SCAGLIA H et al.1977; ACTA ENDOCRINOL.; DANEM.; DA. 1977; VOL. 84; NO 1; PP. 191-199; BIBL. 27 REF.Article

PROBLEMES DIAGNOSTIQUES POSES PAR L'HYPOPARATHYROIDIE PRIMITIVE IDIOPATHIQUE.JUNGEN KETFI M.1976; NANCY; NANCY-THESES; DA. 1976; PP. 1-166; BIBL. 18 P. 1/2; (THESE DOCT. MED.; NANCY I)Thesis

THE LAURENCE-MOON-BARDET-BIEDL SYNDROME IN SIBS. = LE SYNDROME DE LAURENCE-MOON-BARDET-BIEDL CHEZ DES FRERESTEMTAMY SA; SHALASH BA.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 402-407Article

VIRILISM AS A LATE MANIFESTATION IN THE BARDET-BIEDL SYNDROMEHANUNG RV JR; CARLSON IH; GILBERT EF et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 3; PP. 279-292; BIBL. 44 REF.Article

THE LAURENCE-MOON-BARDET-BIEDL SYNDROME: UNRESPONSIVENESS TO THE ACTION OF TESTOSTERONE, A POSSIBLE MECHANISMGHOLAMALI MOZAFFARIAN; NAKHJAVANI MK; ABDOLREZA FARRAHI et al.1979; FERTIL. AND STERIL.; USA; DA. 1979; VOL. 31; NO 4; PP. 417-422; BIBL. 21 REF.Article

THE RENAL LESION OF THE LAURENCE-MOON-BIEDL SYNDROME. = LA LESION RENALE DU SYNDROME DE LAURENCE-MOON-BIEDLHURLEY RM; DERY P; NOGRADY MB et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 87; NO 2; PP. 206-209; BIBL. 10 REF.Article

ASSESSMENT OF OPHTHALMOLOGIC, ENDOCRINOLOGIC AND GENETIC FINDINGS IN THE BARDET-BIEDL SYNDROME = BILAN DES SIGNES OPHTALMOLOGIQUES, ENDOCRINIENS ET GENETIQUES DANS LE SYNDROME DE BARDET-BIEDLBERGSMA DR; BROWN KS.1975; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1975; NO 340; PP. 132-136; BIBL. 26 REF.Article

Bardet-Biedl syndrome and retinitis punctata albescens in an isolated northern Canadian communityPEARCE, W. G; GILLAN, J. G; BROSSEAU, L et al.Canadian journal of ophthalmology. 1984, Vol 19, Num 3, pp 115-118, issn 0008-4182Article

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progressionJUN CHUL KIM; BADANO, Jose L; LEROUX, Michel R et al.Nature genetics. 2004, Vol 36, Num 5, pp 462-470, issn 1061-4036, 9 p.Article

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)MYKYTYN, Kirk; NISHIMURA, Darryl Y; IANNACCONE, Alessandro et al.American journal of human genetics. 2003, Vol 72, Num 2, pp 429-437, issn 0002-9297, 9 p.Article

The oligogenic properties of Bardet-Biedl syndromeKATSANIS, Nicholas.Human molecular genetics (Print). 2004, Vol 13, pp R65-R71, issn 0964-6906, NS1Article

Obesity in heterozygous carriers of the gene for the Bardet-Biedl syndromeCROFT, J. B; MORRELL, D; CHASE, C. L et al.American journal of medical genetics. 1995, Vol 55, Num 1, pp 12-15, issn 0148-7299Article

Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome lociCARMI, R; ELBEDOUR, K; STONE, E. M et al.American journal of medical genetics. 1995, Vol 59, Num 2, pp 199-203, issn 0148-7299Article

Alström syndrome: a case misdiagnosed as Bardet-Biedl syndromeDYER, D. S; WILSON, M. E; SMALL, K. W et al.Journal of pediatric ophthalmology and strabismus. 1994, Vol 31, Num 4, pp 272-274, issn 0191-3913Article

The human FEM1B gene maps to chromosome 15q22 and is excluded as the gene for Bardet-Biedl syndrome, type 4VENTURA-HOLMAN, T; HAIDER, N. B; MAHER, J. F et al.The American journal of the medical sciences. 2000, Vol 319, Num 4, pp 268-270, issn 0002-9629Article

Anomalies in the permanent dentition and other oral findings in 29 individuals with Laurence-Moon-Bardet-Biedl syndromeBORGSTRÖM, M. K; RIISE, R; TORNQVIST, K et al.Journal of oral pathology & medicine. 1996, Vol 25, Num 2, pp 86-89, issn 0904-2512Article

Les troubles mentaux dans le syndrome de (Laurence Moon) - Bardet - Biedl. Discussion = Mental disorders in the Laurence-Moon-Bardet-Biedl syndrom. DiscussionBIEDER, J; MAES-BIEDER, F; LECUYER et al.Annales médico-psychologiques. 1996, Vol 154, Num 4, pp 264-265, issn 0003-4487Article

I: le syndrome de Bardet-Biedl = I: Bardet Biedl syndromKHAITRINE, L; BADGUERAHANIAN, A; FALLAS, P et al.Bulletin des sociétés d'ophtalmologie de France. 1992, Vol 92, Num 10, issn 0081-1270, p. 919Article

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndromeGREEN, J. S; PARFREY, P. S; HARNETT, J. D et al.The New England journal of medicine. 1989, Vol 321, Num 15, pp 1002-1009, issn 0028-4793Article

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