ESSAI D'UNE NOSOLOGIE GENETIQUE DE L'ATRESIA AURIS CONGENITAPFEIFFER RA.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 2; PP. 165-180; BIBL. 3 P.Article

GENETISCHE ASPEKTE DER INFANTILEN ZEREBRALPARESE. = ASPECTS GENETIQUES DE L'ENCEPHALOPATHIE INFANTILE CHRONIQUEPFEIFFER RA.1978; THERAPIEWOCHE; DTSCH.; DA. 1978; VOL. 28; NO 9; PP. 1835-1837; BIBL. 15 REF.Article

AKROMESOMELER ZWERGWUCHS. = NANISME ACROMESOMELIQUEPFEIFFER RA.1976; FORTSCHR. GEB. ROENTGENSTRAHL. NUKLEARMED.; DTSCH.; DA. 1976; VOL. 125; NO 2; PP. 171-173; ABS. ANGL.; BIBL. 18 REF.Article

THE OTO-ONYCHO-PERONEAL SYNDROME. A PROBABLY NEW GENETIC ENTITYPFEIFFER RA.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 4; PP. 317-320; BIBL. 19 REF.Article

LANGER-GIEDION SYNDROME AND ADDITIONAL CONGENITAL MALFORMATIONS WITH INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 8 46, XY, DEL 8 (Q 13-22)PFEIFFER RA.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 2; PP. 142-146; BIBL. 10 REF.Article

LES OLIGODACTYLIESPFEIFFER RA.1982; JOURNAL DE GENETIQUE HUMAINE; ISSN 0021-7743; CHE; DA. 1982; VOL. 30; NO 4; PP. 293-308; BIBL. 4 P.Conference Paper

ACROFACIAL DYSOSTOSIS (NAGER SYNDROME): SYNOPSIS AND REPORT OF A NEW CASEPFEIFFER RA; STOESS H.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 2; PP. 255-260; BIBL. 28 REF.Article

DAS ROBERTS-SYNDROM BERICHT UEBER EINE BEOBACHTUNG (OHNE ANOMALIE DER CENTROMERREGION) = SYNDROME DE ROBERTS. RAPPORT D'UNE OBSERVATION SANS ANOMALIE DE LA REGION DU CENTROMEREPFEIFFER RA; ZWERNER H.1982; MONATSSCHR. KINDERHEILKD.; ISSN 0026-9298; DEU; DA. 1982; VOL. 130; NO 5; PP. 296-298; ABS. ENG; BIBL. 19 REF.Article

AN ATYPICAL CASE OF COCKAYNE'S SYNDROME = UN CAS ATYPIQUE DE SYNDROME DE COCKAYNEPFEIFFER RA; BACKMANN KD.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 1; PP. 28-32; BIBL. 1P.Serial Issue

LIMB ANOMALIES IN CHROMOSOMAL ABERRATIONS.PFEIFFER RA; SANTELMANN R.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 1; PP. 319-337; BIBL. 5 P. 1/2; (MORPHOG. MALFORM. LIMB. INT. CONF. MORPHOG. MALFORM. 2; TITISEE; 1975)Conference Paper

PARTIAL TRISOMY 15Q1.PFEIFFER RA; KESSEL E.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 1; PP. 77-83; BIBL. 19 REF.Article

GIBT ES EIN SYNDROM NACH ULBRICH UND FEICHTIGER. = EXISTE-T-IL UN SYNDROME D'ULBRICH ET FEICHTIGER.PFEIFFER RA; SLAVAYKOFF H.1975; KLIN. PAEDIATR.; DTSCH.; DA. 1975; VOL. 187; NO 2; PP. 176-180; ABS. ANGL.; BIBL. 21REF.Article

DAS AASE-SYNDROM: AUTOSOMAL-REZESSIV VERERBTE, KONNATAL INSUFFIZIENTE ERYTHROPOESE UND TRIPHALANGIE DER DAUMEN = LE SYNDROME D'AASE: ERYTHROPOIESE INSUFFISANTE CONGENITALE A TRANSMISSION AUTOSOMIQUE RECESSIVE ET TRIPHALANGIE DES POUCESPFEIFFER RA; AMBS E.1983; MONATSSCHRIFT FUER KINDERHEILKUNDE; ISSN 0026-9298; DEU; DA. 1983; VOL. 131; NO 4; PP. 235-237; ABS. ENG; BIBL. 13 REF.Article

MIRROR IMAGE DUPLICATIONS OF CHROMOSOME 21. THREE NEW CASES AND DISCUSSION OF THE MECHANISMS OF ORIGINPFEIFFER RA; LOIDL J.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 361-363; BIBL. 18 REF.Article

AN ATYPICAL CASE OF COCKAYNE'S SYNDROME = UN CAS ATYPIQUE DE SYNDROME DE COCKAYNEPFEIFFER RA; BACKMANN KD.1973; CLIN. GENET.; DANM.; DA. 1973; VOL. 4; NO 1; PP. 28-32; BIBL. 1P.Serial Issue

TANDEM DUPLICATION (5Q 13->22) IN A MENTALLY DEFICIENT GIRLKESSEL E; PFEIFFER RA.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 217-220; BIBL. 14 REF.Article

,XY+DER(11;22)(Q23;Q12) FOLLOWING BALANCED TRANSLOCATION T(11;22)(Q23;Q12) MAT. REMARKS ON THE PROBLEM OF TRISOMY 22.KESSEL E; PFEIFFER RA.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 37; NO 1; PP. 111-116; BIBL. 1 P. 1/2Article

CYTOGENETIC STUDIES IN FAMILIES WITH TWO 47, +21-SIBLINGSDHADIAL R; PFEIFFER RA.1972; J. GENET. HUM.; SUISSE; DA. 1972; VOL. 20; NO 4; PP. 297-322; ABS. FR. ALLEM.; BIBL. 3P.Serial Issue

DAS SYNDROM VON SCHWARTZ-JAMPEL (MYOTONIA CHONDRODYSTROPHICA). = LE SYNDROME DE SCHWARTZ-JAMPEL (MYOTONIE CHONDRODYSTROPHIQUE)PFEIFFER RA; BALIER H; PETERSEN C et al.1977; HELV. PAEDIATR. ACTA; SUISSE; DA. 1977; VOL. 32; NO 3; PP. 251-261; ABS. FR. ANGL.; BIBL. 23 REF.Article

DER PHAENOTYP DER TRISOMIE DES KURZEN ARMS EINES CHROMOSOMS NR. 4 (EIN NEUER FALL MIT T(4P; 11Q)). = LE PHENOTYPE DE LA TRISOMIE DU BRAS COURT D'UN CHROMOSOME NO 4 UN NOUVEAU CAS AVEC T(4P; 11Q))KESSEL E; PFEIFFER RA; KOSENOW W et al.1976; KLIN. PAEDIATR.; DTSCH.; DA. 1976; VOL. 188; NO 3; PP. 215-219; ABS. ANGL.; BIBL. 18 REF.Article

TETRAPHOCOMELIA AND NEONATAL AMEGAKARYOCYTIC THROMBOCYTOPENIA = TETRAPHOCOMELIE ET THROMBOCYTOPENIE AMEGACARYOCYTAIRE NEONATALEPFEIFFER RA; MAINTZ G; HANEKE C et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 17; NO 2; PP. 175-178; BIBL. 7REF.Serial Issue

DAS SYNDROM VON ITO (INCONTINENTIA PIGMENTI ACHROMIANS) = LE SYNDROME ITO (INCONTINENCE PIGMENTAIRE ACHROMATIQUE)PFEIFFER RA; HAPPLE R; STUPPERICH G et al.1976; KLIN. PAEDIATR.; DTSCH.; DA. 1976; VOL. 188; NO 2; PP. 181-185; ABS. ANGL.; BIBL. 23 REF.Article

DEFICIENCY OF COAGULATION FACTORS VII AND X ASSOCIATED WITH DELETION OF A CHROMOSOME 13 (Q34). EVIDENCE FROM TWO CASES WITH 46,XY,T(13;Y)(Q11;Q34)PFEIFFER RA; OTT R; GILGENKRANTZ S et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 358-360; BIBL. 13 REF.Article

BALANCIERTE TRANLOCATION T (15Q-; 16P+) ALS URSACHE HABITUELLER FEHLGEBURTEN = TRANSLOCATION EQUILIBREE T (15Q-; 16P+) COMME CAUSE D'AVORTEMENTS HABITUELSHASEGAWA T; PFEIFFER RA; METZ F et al.1973; GEBURTSH. FRAUENHEILKDE; DTSCH.; DA. 1973; VOL. 33; NO 7; PP. 541-544; ABS. ANGL.; BIBL. 24REF.Article

CYTOLOGICAL ANALYSES OF A 14 P+ VARIANT BY MEANS OF N-BANDING AND COMBINATIONS OF SILVER STAINING AND CHROMOSOME BANDINGSLAU YF; WERTELECKI W; PFEIFFER RA et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 75-82; BIBL. 18 REF.Article