VARIABILITY IN THE SMITH-LEMLI-OPITZ SYNDROME: OVERLAP WITH THE MECKEL SYNDROMELOWRY RB.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 3; PP. 429-433; BIBL. 22 REF.Article

HIRSCHSPRUNG'S DISEASE AND CONGENITAL DEAFNESS = MALADIE DE HIRSCHSPRUNG ET SURDITE CONGENITALELOWRY RB.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 1; PP. 114-115; BIBL. 4REF.Article

THE KLIPPEL-FEIL ANOMALAD AS PART OF THE FETAL ALCOHOL SYNDROME.LOWRY RB.1977; TERATOLOGY; U.S.A.; DA. 1977; VOL. 16; NO 1; PP. 53-56; BIBL. 6 REF.Article

THE NAGER SYNDROME (ACROFACIAL DYSOSTOSIS): EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCE.LOWRY RB.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3C; PP. 195-202; BIBL. 3 REF.Article

FAMILIAL GASTROSCHISIS AND OMPHALOCELELOWRY RB; BAIRD PA.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 3; PP. 517-518; BIBL. 4 REF.Article

SYNDROME OF EPIPHYSEAL DYSPLASIA, SHORT STATURE, MICROCEPHALY AND NYSTAGMUSLOWRY RB; WOOD BJ.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 4; PP. 269-274; BIBL. 6 REF.Article

MULTIPLE EPIPHYSEAL DYSPLASIA AND TURNER SYNDROME VARIANT (45, XO/46, X RING) ASSOCIATED WITH ADVANCED MATERNAL AGE.LOWRY RB; WOOD BJ.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3C; PP. 211-220; BIBL. 1 REF.Article

SYNDROME OF MENTAL RETARDATION, CLEFT PALATE, EVENTRATION OF DIAPHRAGM, CONGENITAL HEART DEFECT, GLAUCOMA, GROWTH FAILURE AND CRANIOSYNOSTOSIS.LOWRY RB; MACLEAN JR.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 203-210; BIBL. 2 REF.Article

PROGRESSIVE HEMIFACIAL ATROPHY (PARRY-ROMBERG SYNDROME) REPORT WITH REVIEW OF GENETICS AND NOSOLOGYLEWKONIA RM; LOWRY RB.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 385-390; BIBL. 2 P.Article

"ALDOLASE A" DEFICIENCY WITH SYNDROME OF GROWTH AND DEVELOPMENTAL RETARDATION, MID-FACIAL HYPOPLASIA, HEPATOMEGALY, AND CONSANGUINEOUS PARENTS.LOWRY RB; HANSON JW.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3A; PP. 222-228Article

SALDINO-NOONAN SHORT RIB-POLYDACTYLY DWARFISM SYNDROME = SYNDROME DE NANISME AVEC POLYDACTYLIE ET COTES COURTES DE SALDINO-NOONANLOWRY RB; WIGNALL N.1975; PEDIATRICS; U.S.A.; DA. 1975; VOL. 56; NO 1; PP. 121-123; BIBL. 5 REF.Article

INCIDENCE OF ALBINISM IN BRITISH COLUMBIA (B.C.). SEPARATION BY HAIRBULB TESTMCLEOD R; LOWRY RB.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 1; PP. 77-80; BIBL. 14 REF.Article

CONGENITAL CONTRACTURAL ARACHNODACTYLY: A SYNDROME SIMULATING MARFAN'S SYNDROME = ARACHNODACTYLIE CONGENITALE CONTRACTURANTE: SYNDROME SIMULANT CELUI DE MARFANLOWRY RB; GUICHON VC.1972; CANAD. MED. ASS. J.; CANADA; DA. 1972; VOL. 107; NO 6; PP. 531-533 (2 P.); BIBL. 5 REF.Serial Issue

INCIDENCE RATES FOR CLEFT LIP AND PALATE IN BRITISH COLUMBIA 1952-71 FOR NORTH AMERICAN INDIAN, JAPANESE, CHINESE AND TOTAL POPULATIONS: SECULAR TRENDS OVER TWENTY YEARS.LOWRY RB; TRIMBLE BK.1977; TERATOLOGY; U.S.A.; DA. 1977; VOL. 16; NO 3; PP. 277-283; BIBL. 25 REF.Article

RING 13 CHROMOSOME ASSOCIATED WITH MICROCEPHALY, CONGENITAL HEGRT DEFECT, INTRAUTERINE GROWTH RETARDATION, AND ABNORMAL SKIN PIGMENTATION.LOWRY RB; DILL FJ.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 216-221Article

HYPOSPADIAS IN SUCCESSIVE GENERATIONS-POSSIBLE DOMINANT GENE INHERITANCELOWRY RB; KLIMAN MR.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 3; PP. 285-288; BIBL. 9 REF.Article

A NEW DWARFING SYNDROME WITH EXTERNE SHORTENING OF HUMERI AN SEVERE COXA VARA = UN NOUVEAU NANISME AVEC RACCOURCISSEMENT SEVERE DES HUMERUS ET COXA VARAPATTERSON C; LOWRY RB.1975; RADIOLOGY; U.S.A.; DA. 1975; VOL. 114; NO 2; PP. 341-342; BIBL. 8REF.Article

BORDERLINE NORMAL INTELLIGENCE IN THE SMITH-LEMLI-OPITZ (RSH) SYNDROMELOWRY RB; SIU LI YONG.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 5; NO 2; PP. 137-143; BIBL. 5 REF.Article

QUADRIPLEGIA IN LARSEN SYNDROME.MUZUMDAR AS; LOWRY RB; ROBINSON CEG et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3C; PP. 202-211; BIBL. 4 REF.Article

ANALYSIS OF URINARY MUCOPOLYSACCHARIDES USING SMALL ION EXCHANGE COLUMNSAPPLEGARTH DA; BOZOIAN G; LOWRY RB et al.1975; CLIN. BIOCHEM.; CANADA; DA. 1975; VOL. 8; NO 3; PP. 151-160; BIBL. 16REFArticle

SYNDROME OF MYOPATHY, SHORT STATURE, SEIZURES, RETINITIS PIGMENTOSA, AND CLEFT LIPS.YONG SL; LOWRY RB; JAN JE et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 210-215Article

COMPARISON OF EXISTING CLASSIFICATIONS FOR CODING CONGENITAL MALFORMATION AND GENETIC SYNDROMES.LOWRY RB; ROCHELEAU J; KEILLOR L et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3A; PP. 53-59; BIBL. 5 REF.Article

MUTANT ALLELE FREQUENCIES IN DOMESTIC CATS OF VANCOUVER, BRITISH COLUMBIA.BLUMENBERG B; LOWRY RB; BLUMENBERG G et al.1977; J. HERED.; U.S.A.; DA. 1977; VOL. 68; NO 5; PP. 333-336; BIBL. 25 REF.Article

SURVIVAL AND SPECTRUM OF ANOMALIES IN THE MECKEL SYNDROMELOWRY RB; HILL RH; TISCHLER B et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 3; PP. 417-421; BIBL. 9 REF.Article

TERTIARY TRISOMY (22Q11Q),47,+DER(22), T(11;22)BIEDERMAN BM; LIN CC; LOWRY RB et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 173-177; BIBL. 34 REF.Article