CHORIOIDEREMIE UND FAMILIENBERATUNG = CHOROIDEREMIE ET ENQUETE FAMILIALEKRUEGER KE; MOELLER W; ZERNAHLE K et al.1972; ACTA OPHTHALMOL.; DANEM.; DA. 1972; VOL. 50; NO 6; PP. 782-792; BIBL. 1P.Serial Issue

FAMILIAL EURYBLEPHARONWOLTER JR.1972; J. PEDIATR. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 9; NO 3; PP. 175-176; BIBL. 9REF.Serial Issue

A SURVEY OF MENTALLY DEFECTIVE PARENTS AND THEIR OFFSPRING. = UNE ETUDE DE PARENTS ARRIERES MENTAUX ET DE LEUR DESCENDANCESCALLY BG.1973; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1973; NO 250; PP. 258-262; BIBL. 6REF.; (C.R. IVE CONGR. INT. GENET. HUM.; PARIS; 1971)Conference Paper

FAMILIAL ASSOCIATIONS IN SARCOIDOSIS. A REPORT TO THE RESEARCH COMMITTEE OF THE BRITISH THORACIC AND TUBERCULOSIS ASSOCIATION1973; TUBERCLE; G.B.; DA. 1973; VOL. 54; NO 2; PP. 87-98; ABS. FR. ESP. ALLEM.; BIBL. 2P.1/2Serial Issue

FAMILY WITH PROBABLE ACHONDROGENESIS AND LIPID INCLUSIONS IN FIBROBLASTS = ACHONDROGENESE PROBABLE ET INCLUSIONS LIPIDIQUES DANS LES FIBROBLASTES DANS UNE FAMILLELAXOVA R; OHARA PT; RIDLER MAC et al.1973; ARCH. DIS. CHILDH.; G.B.; DA. 1973; VOL. 48; NO 3; PP. 212-216; BIBL. 7REF.Serial Issue

IGG MONOCLONAL GAMMAPATHY IN THE SISTER OF A PATIENT WITH WALDENSTROEM'S MACROGLOBULINAEMIA = GAMMAPATHIE IGG MONOCLONALE CHEZ LA SOEUR D'UN PATIENT ATTEINT DE MACROGLOBULINEMIE DE WALDENSTROEMFINE JM; LAMBIN P; VALENTIN L et al.1973; BIOMEDICINE; FR.; DA. 1973; VOL. 19; NO 3; PP. 117-121; ABS. FR.; BIBL. 35REF.Serial Issue

3 KINDER MIT CRI-DU-CHAT-SYNDROM = 3 ENFANTS PORTEURS DU SYNDROME DU CRI-DU-CHATPICHLER E; SCHEIBENREITER S.1973; WIEN. MED. WSCHR.; OESTERR.; DA. 1973; VOL. 123; NO 1-2; PP. 19-21; BIBL. 5REF.Serial Issue

A PROPOS D'UN CAS DE MYASTHENIE A DEBUT NEO-NATAL (MYASTHENIE CONGENITALE)CASTANIER L; LELIEVRE GASSIN C.1973; J. MED. STRASBOURG; FR.; DA. 1973; VOL. 4; NO 2; PP. 117-123; ABS. ANGL.; BIBL. 16REF.Serial Issue

FREQUENCE DU PSORIASIS EN FONCTION DE L'AGE1972; VEST. DERMATOL. VENEROL.; S.S.S.R.; DA. 1972; VOL. 46; NO 5; PP. 18-21; ABS. ANGL.; BIBL. 1/2P.Serial Issue

FANCONI'S ANAEMIABEARD MEJ; YOUNG DE; BATEMAN CJT et al.1973; QUART. J. MED.; G.B.; DA. 1973; VOL. 42; NO 166; PP. 403-422; BIBL. 1P.Serial Issue

HAEMOGLOBIN H DISEASE IN A TURKISH FAMILY = HEMOGLOBINOSE H DANS UNE FAMILLE TURQUEOZSOYLU S; ISIK K.1973; SCAND. J. HAEMATOL.; DENM.; DA. 1973; VOL. 10; NO 1; PP. 54-58; BIBL. 1P.Serial Issue

HEREDOBIOLOGICAL PROBLEMS RELATED WITH THYROID AUTOIMMUNITY = ASPECTS BIOLOGIQUES HEREDITAIRES DE L'AUTO-IMMUNITE THYROIDIENNESIMIONESCU L; SAHLEANU V.1973; REV. ROUMAINE ENDOCRINOL.; ROUMAN.; DA. 1973; VOL. 10; NO 2; PP. 121-131Article

POLYMORPHISM OF HUMAN C-BAND HETEROCHROMATIN. I. FREQUENCY OF VARIANTS = POLYMORPHISME DE L'HETEROCHROMATINE DES BANDES C HUMAINES. I. FREQUENCE DES VARIANTESCRAIG HOLMES AP; MOORE FB; SHAW MW et al.1973; AMER. J. HUM. GENET.; U.S.A.; DA. 1973; VOL. 25; NO 2; PP. 181-192; BIBL. 17REF.Serial Issue

VALUE OF TWIN STUDIES IN DERMATOLOGICAL GENETICS = VALEUR DE L'ETUDE DES JUMEAUX EN DERMATOLOGIE GENETIQUECAVALIERI R.1973; INTERNATION. J. DERMATOL.; U.S.A.; DA. 1973; VOL. 12; NO 1; PP. 29-34; BIBL. 7REF.Serial Issue

SCLEROSE EN PLAQUES ET FAMILLEBOUCHE B; BELANGER C; SAINT HILAIRE JM et al.1972; LYON MEDITERR. MED.; FR.; DA. 1972; VOL. 8; NO 23; PP. 2209-2224 (9 P.); BIBL. 34 REF.Serial Issue

ABERRATIONS CHROMOSOMIQUES CHEZ LES PARENTS DANS DES CAS D'AVORTEMENTS SPONTANES REPETESKULAZHENKO VP; LAZYUK GI; LEVCHENKO NN et al.1972; GENETIKA; S.S.S.R.; DA. 1972; VOL. 8; NO 7; PP. 154-164; ABS. ANGL.; BIBL. 1P.1/2Serial Issue

FAMILIAL OCCURRENCE OF SARCOIDOSIS = SURVENUE FAMILIALE DE LA SARCOIDOSEWIMAN LG.1972; SCAND. J. RESP. DIS., SUPPL.; DENM.; DA. 1972; NO 80; PP. 115-119; BIBL. 5REF.; (PROC. INT. CONF. PULM. DIS.; AULANKO; 1971)Conference Paper

THE MENTAL HEALTH OF SIBLINGS OF CONGENITALLY ABNORMAL CHILDREN = LA SANTE MENTALE DES FRERES ET SOEURS D'ENFANTS AYANT DES MALFORMATIONS CONGENITALESGATH A.1972; J. CHILD PSYCHOL. PSYCHIATRY; G.B.; DA. 1972; VOL. 13; NO 3; PP. 211-218; BIBL. 10REF.Article

LE PRONOSTIC GENETIQUE EN OPHTALMOLOGIEFRANCOIS J.1972; ANNEE THERAPEUT. CLIN. OPHTALMOL.; FR.; DA. 1972; VOL. 23; PP. 319-330Serial Issue

RECHERCHES CYTOGENETIQUES CHEZ LES ENFANTS ATTEINTS DU SYNDROME DE DOWN ET CHEZ LEURS PARENTSOSTOJSKA J.1972; PEDIATR. POLSKA; POLSKA; DA. 1972; VOL. 47; NO 10; PP. 1231-1238; ABS. RUSSE ANGL.; BIBL. 26REF.Serial Issue

DEVELOPMENT OF CHILDHOOD ALLERGY IN INFANTS FED BREAST, SOY, OR COW MILKHALPERN SR; SELLARS WA; JOHNSON RB et al.1973; J. ALLERGY CLIN. IMMUNOL.; U.S.A.; DA. 1973; VOL. 51; NO 3; PP. 139-151; BIBL. 1P.Serial Issue

GENETIC MAPPING IN MAN.RENWICK JH.1973; PROC. R. SOC. MED.; G.B.; DA. 1973; VOL. 66; NO 3; PP. 275-276; BIBL. 8REF.Serial Issue

GENETIC THYREOPATHIES = PATHOLOGIE THYROIDIENNE D'ORIGINE GENETIQUENEGOESCU I; MUSETEANU P; MAXIMILIAN C et al.1973; REV. ROUMAINE ENDOCRINOL.; ROUMAN.; DA. 1973; VOL. 10; NO 2; PP. 101-112Article

IRIS DYSPLASIA, ORBITAL HYPERTELORISM, AND PSYCHOMOTOR RETARDATION: A DOMINANTLY INHERITED DEVELOPMENTAL SYNDROME = DYSPLASIE IRIENNE, HYPERTELORISME ORBITAIRE ET ARRIERATION PSYCHO-MOTRICE: UN SYNDROME HEREDITAIRE DOMINANT DE DEVELOPPEMENTDE HAUWERE RC; LEROY JG; ADRIAENSSENS K et al.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 4; PP. 679-681; BIBL. 7REF.Serial Issue

PATERNAL TRISOMY 21 MOSAICISM AND DOWN'S ANOMALY = MOSAIQUE PATERNELLE AVEC TRISOMIE 21 ET ANOMALIE DE DOWNMEHES K.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 17; NO 4; PP. 297-300; ABS. ALLEM.; BIBL. 8REF.Serial Issue