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A PROPOS D'UNE OBSERVATION DE MALADIE DU CRI DU CHAT.CASTEL Y; TOUDIC L; RIVIERE D et al.1977; REV. INTERNATION. PEDIATR.; FR.; DA. 1977; NO 76; PP. 29-42; BIBL. 19 REF.Article

CYTOGENETIC RECOMBINANTS FROM A FEMALE CARRYING A PARACENTRIC INVERSION OF THE SHORT ARM OF CHROMOSOME NUMBER 5VALCARCEL E; BENITEZ J; MARTINEZ P et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 78-81; BIBL. 12 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME 5 FROM A SUBJECT WITH CRI-DU-CHAT SYNDROME. REPOSITORY IDENTIFICATION NO. GM71.BREG WR; ARONSON MM; GREENE AE et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 4; PP. 239-240; BIBL. 3 REF.Article

DEL (5P) WITHOUT "CRI DU CHAT" PHENOTYPEBACCICHETTI C.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 4; PP. 389Article

CYTOGENETIQUE DU SYNDROME DU CRI DU CHATZHOU HUANGENG; KANG XUEZHEN; ZHANG QIANQIAN et al.1982; ACTA GENET. SIN.; CHN; DA. 1982; VOL. 9; NO 1; PP. 20-23; ABS. ENG; BIBL. 7 REF.Article

FETAL MANIFESTATION OF CHROMOSOMAL DISORDER: PARTIAL DUPLICATION OF THE LONG ARM OF CHROMOSOME 5 (5Q33->QTER)PASSARGE E; BARTSCH SANDHOFF M; REHDER H et al.1982; TERATOLOGY; ISSN 0040-3709; USA; DA. 1982; VOL. 25; NO 2; PP. 221-225; BIBL. 15 REF.Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 5 IN A DEFORMED BOY: 46,XY,DEL(5) (Q13Q15)STOLL C; LEVY JM; ROTH MP et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 6; PP. 486-487; BIBL. 4 REF.Article

DERMATOGLYPHICS IN CRI DU CHAT SYNDROME.SHIONO H; KADOWAKI JI; KAZAMA H et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 214-218; BIBL. 1 P.Article

CONSIDERAZIONI SU CINQUE CASI DI SINDROMI DI CRI DU CHAT. = DISCUSSIONS CONCERNANT CINQ CAS DE SYNDROME DU CRI DU CHATCERRUTI MAINARDI C; VIANELLO MG; BONIOLI E et al.1976; MINERVA PEDIATR.; ITAL.; DA. 1976; VOL. 28; NO 38; PP. 2389-2400; ABS. ANGL.; BIBL. 1 P.Article

PARTIAL TRISOMIE 5Q: THREE DIFFERENT PHENOTYPES DEPENDING ON DIFFERENT DUPLICATION SEGMENTSRODEWALD A; ZANKL M; GLEY EO et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 2; PP. 191-198; BIBL. 8 REF.Article

PRENATAL DIAGNOSIS OF 5 P.DAVID K; KAFFE S; STRAUSS L et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 2; PP. 224-228; BIBL. 12 REF.Article

THE HETEROGENEITY OF THE 5Q-CHROMOSOME MARKER IN REFRACTORY ANEMIA = L'HETEROGENEITE DU MARQUEUR CHROMOSOMIQUE-5Q DANS L'ANEMIE REFRACTAIREWATT JL; KING DJ; PALMER JBD et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 9; NO 2; PP. 113-118; ABS. ENG; BIBL. 13 REF.; FIGArticle

INTERSTITIAL DELETION IN THE LONG ARM OF CHROMOSOME NO.5HARPRECHT BEATO W; KAISER P; STEUBER E et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 2; PP. 167-171; BIBL. 8 REF.Article

UNUSUAL OCULAR FINDINGS IN AN INFANT WITH CRI-DU-CHAT SYNDROMEKITSIOU TZELI S; DELLAGRAMMATICAS HD; PAPAS CB et al.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 4; PP. 304-307; BIBL. 5 REF.Article

THE 5Q-CHROMOSOME IN A CASE OF ERYTHROID HYPOPLASIAHARTLEY SE; MCCALLUM CJ.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 1; PP. 33-36; BIBL. 9 REF.Article

45,X CONSTITUTION IN A H-Y ANTIGEN POSITIVE BOY WITH PARTIAL MONOSOMY 5PSEIDEL H; MILLER K; SPOLIAR M et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 4; PP. 290-297; BIBL. 12 REF.Article

GENETIC MARKERS IN INDIVIDUALS WITH A 5 P-KARYOTYPEFENGER K; MOHL IA.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 1; PP. 58-59; BIBL. 4 REF.Article

CYTOLOGIC OBSERVATIONS IN 35 INDIVIDUALS WITH A 5P-KARYOTYPE.NIEBUHR E.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 42; NO 2; PP. 143-156; BIBL. 29 REF.Article

A (5; 14) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-589.BORGAONKAR DS; ARONSON MM; GREENE AE et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 242Article

A CHILD WITH INTERSTITIAL DELETION OF CHROMOSOME NO 5FELDING I; KRISTOFFERSON U.1980; HEREDITAS; ISSN 0018-0661; SWE; DA. 1980; VOL. 93; NO 2; PP. 337-339; BIBL. 2 REF.Article

RING CHROMOSOME 5 IN TWO MALFORMED BOYS WITH CRI DU CHAT SYNDROMESUERINCK E; NOEL B; RETHORE MO et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 125-129; BIBL. 5 REF.Article

SUPERNUMERARY SMALL CHROMOSOMAL ANOMALY: REPORT OF THREE CASES INCLUDING ONE WITH A FAMILIAL INVERSION OF CHROMOSOME 5HING LIANG LEE; SCHNEIDER J; WASANT P et al.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 3; PP. 275-285; ABS. FRE/GER; BIBL. 16 REF.Article

SYNDROME DYSMORPHIQUE, DEBILITE MENTALE ET DELETION INTERSTITIELLE DES BRAS LONGS D'UN CHROMOSOME 5PESCIA G; GAIDE AC; JUILLARD E et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 3; PP. 161-163; ABS. ENG; BIBL. 8 REF.Article

THE LARYNX IN THE CRI DU CHAT SYNDROME.MANNING KP.1977; J. LARYNGOL. OTOL.; G.B.; DA. 1977; VOL. 91; NO 10; PP. 887-892; BIBL. 22 REF.Article

THE 5Q-CHROMOSOME ABNORMALITY IN HAEMATOLOGICAL DISORDERS: A COLLABORATIVE STUDY OF 34 CASES FROM THE NETHERLANDSKERKHOFS H; HAGEMEIJER A; LEEKSMA CHW et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 3; PP. 365-381; BIBL. 2 P.Article

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