MALADIE DE BASEDOW FAMILIALE PORTANT SUR TROIS GENERATIONSGILBERT DREYFUS; PEILLON F; DOUCET D et al.1972; ANN. MED. INTERNE; FR.; DA. 1972; VOL. 123; NO 11; PP. 937-940; BIBL. 11REF.Article

SARKOIDOSE BEI GESCHWISTERN = SARCOIDOSE DANS UNE FRATRIEVOLKMAR W; SEIDEL R.1972; DTSCHE GESUNDH.-WES.; DTSCH.; DA. 1972; VOL. 27; NO 32; PP. 1491-1496; ABS. RUSSE ANGL.; BIBL. 52REF.Serial Issue

REPORT OF THE FAMILIAL OCCURRENCE OF SYSTEMIC LUPUS ERYTHEMATOSUS IN MALE SIBLINGS = SURVENUE FAMILIALE DE LUPUS ERYTHEMATEUX DISSEMINE CHEZ DES FRERESSPECTOR DA; JAMPOL LM; HAYSLETT JP et al.1973; ARTHRIT. AND RHEUMATISM; U.S.A.; DA. 1973; VOL. 16; NO 2; PP. 221-224; BIBL. 20REF.Serial Issue

FAMILIAL GOITROUS CRETINISM = CRETINISME FAMILIAL AVEC GOITRENIRMALA VASHI.1972; INDIAN PEDIATR.; INDIA; DA. 1972; VOL. 9; NO 11; PP. 697-702; H.T. 1; BIBL. 19REF.Article

PHEOCHROMOCYTOME FAMILIALSERINGE P; PERELMAN R; PLAINFOSSE B et al.1972; ANN. ENDOCRINOL.; FR.; DA. 1972; VOL. 33; NO 5; PP. 529-530; ABS. ANGL.Article

FAMILIAL OCCURRENCE OF CONGENITAL ABSENCE OF THE VAGINAJONES HW JR; MERMUT S.1972; AMER. J. OBSTETR. GYNECOL.; U.S.A.; DA. 1972; VOL. 114; NO 8; PP. 1100-1101; BIBL. 4 REF.Article

La psychogénéalogie : À la recherche des racines familiales de la maladieROOBAERT, V.Louvain médical. 2006, Vol 125, Num 7, pp 245-251, issn 0024-6956, 7 p.Article

Anomalies héréditaires de l'oxydation mitochondriale des acides grasBONNEFONT, J.P; MITCHELL, G; COLONNA, M et al.LA MEDECINE INFANTILE. 1990, Vol 2, Num 02, pp 113-123Article

Anomalies héréditaires de l'oxydation mitochondriale des acides grasBONNEFONT, J.P; MITCHELL, G; COLONNA, M et al.LA MEDECINE INFANTILE. 1990, Vol 2, Num 02, pp 113-123Article

FAMILIAERE GLUCOCORTICOIDINSUFFIZIENZ = L'INSUFFISANCE GLUCOCORTICOIDIENNE FAMILIALEPETRYKOWSKI WV; BURMEISTER P; BOHM N et al.1975; KLIN. PAEDIATR.; DTSCH.; DA. 1975; VOL. 187; NO 3; PP. 198-215; ABS. ANGL.; BIBL. 37REF.Article

UN PARTICOLARE CASO DI IPERCHERATOSI PALMOPLANTARE = CAS PARTICULIER D'HYPERKERATOSE PALMOPLANTAIREFALDARINI G; FUSI F.1972; G. ITAL. DERMATOL., MINERVA DERMATOL.; ITAL.; DA. 1972; VOL. 107; NO 5; PP. 180-182; ABS. ANGL.; BIBL. 3 REF.Serial Issue

ACRODYNIE CHEZ 2FRERES1972; PEDIATR. POLSKA; POLSKA; DA. 1972; VOL. 47; NO 6; PP. 765-767; ABS. RUSSE ANGL.; BIBL. 7REF.Serial Issue

LUPUS ERYTHEMATEUX SYSTEMIQUE CHEZ DES JUMEAUX UNIVITELLIUSPETROVA TR; AKOPOVA VL.sdTERAP. ARKH.; S.S.S.R.; DA. 197; VOL. 44; NO 5; PP. 111-113; ABS. ANGL.; BIBL. 1 REF.Serial Issue

BILATERAL BREAST CANCER, CLINICAL AND PATHOLOGICAL REVIEW = CANCER BILATERAL DU SEIN. REVUE CLINIQUE ET ANATOMO-PATHOLOGIQUEFINNEY GG JR; FINNEY GG; MONTAGUE ACW et al.1972; ANN. SURG.; U.S.A.; DA. 1972; VOL. 175; NO 5; PP. 635-646; BIBL. 14REF.Article

BILATERAL PHAEOCHROMOCYTOMA IN TWO BROTHERS = PHEOCHROMOCYTOME BILATERAL CHEZ DEUX FRERESSTRUNGE P; INGSTRUP HM; LOECHTE JJ et al.1972; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1972; VOL. 61; NO 6; PP. 729-732; BIBL. 14 REF.Article

FAMILIAL HYPERPARATHYROIDISM. MILD HYPERCALCEMIA IN AT LEAST NINE MEMBERS OF A KINDRED = HYPERPARATHYROIDISME FAMILIAL. HYPERCALCEMIE MODEREE CHEZ AU MOINS NEUF PERSONNES D'UNE MEME LIGNEEMARX SJ; POWELL D; SHIMKIN PM et al.1973; ANN. INTERN. MED.; U.S.A.; DA. 1973; VOL. 78; NO 3; PP. 371-377; BIBL. 35REF.Article

CONGENITAL SCALP DEFECTS IN BROTHER AND SISTER = PERTES DE SUBSTANCE CONGENITALES DU CUIR CHEVELU CHEZ FRERE ET SOEUR1972; MED. J. AUSTRAL.; AUSTRAL.; DA. 1972; VOL. 59; NO 17; PP. 866-868; BIBL. 16REF.Serial Issue

WART-LIKE POROKERATOSIS OF MIBELLI = POROKERATOSE PSEUDO-VERRUQUEUSE DE MIBELLIENG AM.1973; ACTA DERMATO-VENEREOL.; SUEDE; DA. 1973; VOL. 53; NO 2; PP. 157-159; BIBL. 15REF.Serial Issue

URTICARIA PIGMENTOSA BEI EINEIIGEN ZWILLINGEN = URTICAIRE PIGMENTAIRE CHEZ DEUX JUMELLES1973; DERMATOL. MONATSSCHR.; DTSCH.; DA. 1973; VOL. 159; NO 3; PP. 258-261; ABS. ANGL.; BIBL. 15REF.Serial Issue

ASSOCIATION OF SOFT TISSUE SARCOMA, LEUKEMIA AND BRAIN TUMORS IN FAMILIES AFFECTED WITH BREAST CANCERLYNCH HT; KRUSH AJ; HARLAN WL et al.1973; AMER. SURGEON; U.S.A.; DA. 1973; VOL. 39; NO 4; PP. 199-206; BIBL. 15REF.Article

CANCER DU LARYNX CHEZ LA MERE ET LA FILLEPERRIN C; GENETET B; MASSON JP et al.1972; J. FR. OTO-RHINO-LARYNGOL.; FR.; DA. 1972; VOL. 21; NO 10; PP. 941-946 (4 P.)Serial Issue

HYPERKERATOSE PILIFORME DISSEMINEE FAMILIALEAUFGANG A.1972; ANN. DERMATOL. SIPHILIGR.; FR.; DA. 1972; VOL. 99; NO 4; PP. 381-390; ABS. ANGL.; BIBL. 6 REF.Serial Issue

THE PATHOGENESIS OF GRAVES' DISEASE. A DISORDER OF DELAYED HYPERSENSITIVITY.VOLPE R; EDMONDS M; LAMKI L et al.1972; MAYO CLIN. PROC.; U.S.A.; DA. 1972; VOL. 47; NO 11; PP. 824-834; BIBL. 1 P. 1/2Article

Absence of consensus in diagnostic criteria for familial neurodegenerative diseasesBYRNE, Susan; ELAMIN, Marwa; BEDE, Peter et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 4, pp 365-367, issn 0022-3050, 3 p.Article

LA MALADIE DE BASEDOW FAMILIALE. (A PROPOS DE DIX-HUIT CAS DANS HUIT FAMILLES)COURT NJM.1972; GRENOBLE; IMPR. COMMEROT; DA. 1972; PP. 1-46; BIBL. 11 P.; (THESE DOCT. MED., UNIV. CLAUDE BERNARD LYON, 1972)Thesis