GENETIC DISEASES OF METABOLISMRAIVIO KO; SEEGMILLER JE.1972; ANNU. REV. BIOCHEM.; U.S.A.; DA. 1972; VOL. 41; PP. 543-576; BIBL. 7P.Serial Issue

VARIABILITY OF ARTERIAL PRESSURE IN NORMOTENSIVE AND SPONTANEOUSLY HYPERTENSIVE RATS = VARIABILITE DE LA P ARTERIELLE CHEZ DES RATS PRESENTANT UNE TENSION ARTERIELLE NORMALE OU UNE HYPERTENSION SPONTANEEFROHLICH ED; PFEFFER MA; WEISS AK et al.1972; PROC. SOC. EXPER. BIOL. MED.; U.S.A.; DA. 1972; VOL. 140; NO 1; PP. 145-148; BIBL. 11REF.Serial Issue

INSULINSEKRETION UND GLUKOSETOLERANZ BEI TIEREXPERIMENTELLER HYPERTONIE. I. UNTERSUCHUNGEN BEIM GENETISCH BEDINGTEN SPONTANEN HYPERTONUS DER RATTE = LA SECRETION INSULINIQUE ET LA TOLERANCE AU GLUCOSE I.V. DANS L'HYPERTENSION EXPERIMENTALE. I. ETUDES DANS L'HYPERTENSION SPONTANEE D'ORIGINE GENETIQUE DU RATWAGNER H; WESSELS F; ZIERDEN E et al.1972; MED. WELT; DTSCH.; DA. 1972; NO 25; PP. 907-910Serial Issue

LATE INFANTILE METACHROMATIC LEUCODYSTROPHY. REPORT OF 2CASES AND REVIEW OF IN VIVO DIAGNOSTIC TESTS = LA LEUCODYSTROPHIE METACHROMATIQUE INFANTILE D'APPARITION TARDIVE. RAPPORT DE 2CAS ET REVUE DES TESTS DIAGNOSTIQUES IN VIVOTHUNOLD S.sdBEITR. PATHOL.; DTSCH.; DA. 197; VOL. 146; NO 4; PP. 322-331; BIBL. 1P.Serial Issue

A GUIDE TO SCREENING NEWBORN INFANTS FOR INBORN ERRORS OF METABOLISM = UN GUIDE POUR DEPISTER LES ERREURS CONGENITALES DU METABOLISME CHEZ LES NOUVEAU-NESBUIST NRM; JHAVERI BM.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 3; PP. 511-522; BIBL. 1P.Serial Issue

HEREDODEGENERATIVE DISEASES OF THE CHILDREN'S NERVOUS SYSTEM = MALADIES HEREDO-DEGENERATIVES DU SYSTEME NERVEUX DE L'ENFANT1971; IN: IIND PRAGUE INST. SYMP. CHILD NEUROL., PRAGUE, 1970; PRAHA; UNIV. KARLOVA; DA. 1971; PP. 11-42; BIBL. DISSEM.Conference Proceedings

SCREENING FOR METABOLIC DISORDERS ASSOCIATED WITH MENTAL RETARDATION = DETECTION DES DESORDRES METABOLIQUES ASSOCIES A UN RETARD MENTALHILL A; ZALESKI WA.1972; CLIN. BIOCHEM.; CANADA; DA. 1972; VOL. 5; NO 1; PP. 33-45; BIBL. 1 P. 1/2Serial Issue

ROENTGEN FINDINGS IN MUCOLIPIDOSISIII. (PSEUDO-HURLER POLYDYSTROPHY = CONSTATATIONS RADIOLOGIQUES DANS LA MUCOLIPIDOSEIII. (PSEUDO-POLYDYSTROPHIE DE HURLER)MELHEM R; DORST JP; SCOTT CI JR et al.1973; RADIOLOGY,; U.S.A.; DA. 1973; VOL. 106; NO 1; PP. 153-160; BIBL. 15REF.Serial Issue

HYPERCONCAVITE (SCALLOPING) VERTEBRALE LOMBAIRE AU COURS DE LA MALADIE DE RECKLINGHAUSENDEBAENE A; ACQUAVIVA P; DUFOUR M et al.1973; J. RADIOL. ELECTROL. MED. NUCL.; FR.; DA. 1973; VOL. 54; NO 2; PP. 149-191; ABS. ANGL.; BIBL. 3REF.Serial Issue

SAISONALER PRURITUS ALS SYMPTOM DER ERYTHROPOETISCHEN PROTOPORPHYRINAEMISCHEN LICHTDERMATOSE. (EPL) = PRURIT SAISONNIER, SYMPTOME DE LA DERMATOSE ACTINIQUE ERYTHROPOIETIQUE PROTOPORPHYRINEMIQUEBURG G; PLEWIG G.1972; HAUTARZT; DTSCH.; DA. 1972; VOL. 23; NO 12; PP. 553-55; BIBL. 15REF.Serial Issue

THE OCULAR HISTOPATHOLOGY OF HOMOCYSTINURIA. A LIGHT AND ELECTRON MICROSCOPIC STUDYRAMSEY MS; YANOFF M; FINE BS et al.1972; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1972; VOL. 74; NO 3; PP. 377-385; BIBL. 25 REF.Serial Issue

MENKES'S KINKY HAIR SYNDROME. AN INHERITED DEFECT IN COPPER ABSORPTION WITH WIDESPREAD EFFECTS = SYNDROME DES CHEVEUX CREPELES DE MENKES. UN DEFAUT HEREDITAIRE DE L'ABSORPTION DU CUIVRE A EFFETS MULTIPLESDANKS DM; CAMPBELL PE; STEVENS BJ et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 2; PP. 188-201; BIBL. 20 REF.Serial Issue

PALMAR DERMATOGLYPHS IN TUBEROUS SCLEROSIS = DERMATOGLYPHES PALMAIRES DANS LA SCLEROSE TUBEREUSE1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 443-447; BIBL. 14REF.Serial Issue

EPILEPSIE AVEC TROUBLES DU METABOLISME DU PHOSPHORE CHEZ LES ENFANTSOBINTSOVA SS.1972; TRUDY LENINGRAD. NAUCH.-ISSLEDOVAT. PSIKHONEVROL. INST. V.M. BEKHTEREVA; S.S.S.R.; DA. 1972; VOL. 61; PP. 92-95; BIBL. 6REF.Serial Issue

POSSIBLE GENETIC CONSEQUENCES OF RELAXED SELECTION AGAINST COMMON DISORDERS WITH COMPLEX INHERITANCEMATSUNAGA E.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 1; PP. 53-57; BIBL. 6 REF.Article

THE IMPORTANCE OF DETERMINING THE MODE OF INHERITANCE FOR THE ESTIMATION OF RECURRENCE RISKSVAN REGEMORTER N; SMITH C.1976; J. GENET. HUM.; SUISSE; DA. 1976; VOL. 24; NO 1; PP. 49-60; ABS. FR. ALLEM.; BIBL. 1 P. 1/2Article

MOEGLICHKEITEN UND GRENZEN DER GENETISCHEN BERATUNG IN DER BUNDESREPUBLIK = POSSIBILITES ET LIMITES DU CONSEIL GENETIQUE EN REPUBLIQUE FEDERALEWENDT GG.1976; MUENCH. MED. WSCHR.; DTSCH.; DA. 1976; VOL. 118; NO 19; PP. 587-588; BIBL. 6 REF.Article

MUENCHMEYER-SYNDROM (FIBRODYSPLASIA ("MYOSITIS") OSSIFICANS PROGRESSIVA) = SYNDROME DE MUENCHMEYER (MYOSITE OSSIFIANTE PROGRESSIVE)WIEDEMANN HR; DIBBERN H; GROSSE FR et al.1976; MED. WELT; DTSCH.; DA. 1976; VOL. 27; NO 5; PP. 194-195Article

DISTRIBUTION OF SIBSHIP SIZE IN FAMILIES MANIFESTING A GENETICALLY DETERMINED DISORDER. = REPARTITION DE LA TAILLE DE LA FRATRIE DANS DES FAMILLES PRESENTANT UN DESORDRE GENETIQUEMAYO O.1975; HUM. HERED.; SWITZ.; DA. 1975; VOL. 25; NO 2; PP. 127-134; BIBL. 13 REF.Article

ERITROQUERATODERMIA VARIABLE EN "COCARDAS" DE DEGOS = ERYTHROKERATODERMIE VARIABLE EN "COCARDES" DE DEGOSBEZERRA L.1975; DERMATOLOGIA; MEX.; DA. 1975; VOL. 19; NO 1; PP. 82Article

HISTOMETRISCHE BEFUNDE AN NEBENNIEREN VON HAUSSCHWEINEN IM HINBLICK AUF KONSTITUTIONSMAENGEL = DONNEES HISTOMETRIQUES CONCERNANT LA SURRENALE DU PORC DOMESTIQUE, EN CE QUI CONCERNE LES DEFICIENCES CONSTITUTIONNELLESHAID H.1975; Z. MIKR.-ANAT. FORSCH.; DTSCH.; DA. 1975; VOL. 89; NO 3; PP. 479-485; ABS. ANGL.; BIBL. 16 REF.Article

GENODERMATOSES AND CONGENITAL DISORDERS1972; YB. DERMATOL.; U.S.A.; DA. 1972; PP. 146-178; BIBL. 1P. 1/2Serial Issue

LES ANOMALIES HEREDITAIRES DES ENZYMES DIGESTIVES1972; MED. CHIR. DIGEST.; FR.; DA. 1972; VOL. 1; NO 1; PP. 41-44; BIBL. 9REF.Serial Issue

METHODOLOGY OF THE QUANTITATIVE CYTOCHEMICAL ANALYSIS OF SINGLE OR SMALL NUMBERS OF CULTURED CELLS = METHODOLOGIE DE L'ANALYSE CYTOCHIMIQUE QUANTITATIVE DE CELLULES EN CULTURE ISOLEES OU EN PETIT NOMBREGALJAARD H; VAN HOOGSTRATEN JJ; DE JOSSELIN DE JONG JE et al.1974; HISTOCHEM. J.; G.B.; DA. 1974; VOL. 6; NO 4; PP. 409-429; BIBL. 2P.1/2Article

LES ICHTYOSESRIMBAUD P; MEYNADIER J; GUILHOU JJ et al.1972; CAH. MED.; FR.; DA. 1972; VOL. 13; NO 15-16; PP. 1095-1100; BIBL. 31REF.Serial Issue