kw.\*:("CHROMOSOME B4 ANORMAL")
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A (4;15) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-624KOHN G; COHEN MM; ARONSON M et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 2; PP. 124-125Article
SINDROMES 4P-Y 5P-(SU IDENTIFICACION POR EL ESTUDIO CROMOSOMICO). = SYNDROMES 4P- ET 5P. LEUR IDENTIFICATION PAR L'ETUDE CHROMOSOMIQUEPRIETO F; BADIA L; ORELLANA F et al.1975; REV. ESP. PEDIATR.; ESP.; DA. 1975; VOL. 31; NO 184; PP. 581-590; ABS. FR. ANGL. ALLEM.; BIBL. 1 P.Article
A (4;21) TRANSLOCATION, UNBALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-98SEABRIGHT M; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 152-153Article
A (4;11) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-380KOUSSEFF BG; KIM HJ; HSU LYF et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 150-151Article
THE PARTIAL 4Q MONOSOMY. REPORT OF A 5-YEAR-OLD BOY WITH DELETION 4Q31.3->4Q TERSANDIG KR; MUECKE J; TRAUTMANN U et al.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 3; PP. 254-257; BIBL. 11 REF.Article
MEIOTIC CHROMOSOME STUDY IN A HUMAN FEMALE TRANSLOCATION HETEROZYGOTE = ETUDE DES CHROMOSOMES EN MEIOSE CHEZ UNE FEMME PORTEUSE D'UNE TRANSLOCATION HETEROZYGOTEUEBELE KALLHARDT B; KNOERR K.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 4; PP. 355-356; BIBL. 3 REF.Article
THE WOLF-HIRSCHHORN (4P-) SYNDROME.JOHNSON VP; MULDER RD; HOSEN R et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 2; PP. 104-112; BIBL. 2 P.Article
TWO CHILDREN WITH DELETION OF THE LONG ARM OF CHROMOSOME 4 WITH BREAKPOINT AT BAND Q33TOMKINS DJ; HUNTER AGW; UCHIDA IA et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 6; PP. 348-355; BIBL. 14 REF.Article
CENTRIC FISSION OF CHROMOSOME NO. 4 IN THE MOTHER OF TWO PATIENTS WITH TRISOMY 4 P.DALLA PICCOLA B; MASTROIACOVO P; GANDINI E et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 1; PP. 121-125; BIBL. 18 REF.Article
THE TRISOMY 4P SYNDROME: A CASE REPORTKEREN G; CHAKI R; KATZNELSON BM et al.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 3; PP. 273-275; BIBL. 6 REF.Article
CYTOLOGICAL ASSESSMENT OF MEIOTIC EXCHANGE IN A HUMAN MALE WITH A PERICENTRIC INVERSION OF CHROMOSOME NO. 4VAN DER LINDEN AGJM; PEARSON PL; VAN DE KAMP JJP et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 2; PP. 126-139; BIBL. 3P.1/2Article
DE NOVO OCCURENCE OF 46,XX,T(4;13)(Q31;Q14) IN A MENTALLY RETARDED GIRLJENKINS EC; CURCURU GIORDANO FM; KRISHNA SG et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 117-120; ABS. FR.; BIBL. 7REF.Article
A FAMILY WITH AN INHERITED TRANSLOCATION INVOLVING THE NO 4/NO. 21 CHROMOSOMESDARMADY JM; SEABRIGHT M.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 408-411; BIBL. 9 REF.Article
INDAGINE NEUROPSICOPATOLOGICA IN 2 CASI DI TRISOMIA 4P = ETUDE NEUROPSYCHOPATHOLOGIQUE DANS 2 CAS DE TRISOMIE 4PGIOVANNELLI G; PEZZANI C; MEDIOLI CAVARA F et al.1974; MINERVA PEDIATR.; ITAL.; DA. 1974; VOL. 26; NO 39; PP. 1933-1943; ABS. ANGL.; BIBL. 11REF.Article
LETTER TO THE EDITOR: DELETION OF CHROMOSOME 4Q33->QTER. IS IT DIFFERENT FROM 4Q31->QTER DELETION SYNDROME.TUCHMAN M; EBRAHIMI J; GORLIN RJ et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 391-393; BIBL. 11 REF.Article
THE DEL(4)(Q31) SYNDROME: A RECOGNIZABLE DISORDER WITH ATYPICAL ROBIN MALFORMATION SEQUENCEDAVIS JM; CLARREN SK; SALK DJ et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 2; PP. 113-117; BIBL. 11 REF.Article
CROSSING-OVER DURING HUMAN SPERMATOGENESIS VISUALIZED CYTOLOGICALLYHANSMANN I; GEISLER M; GRIMM T et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 4; PP. 375-377; BIBL. 18 REF.Article
KING 4 CHROMOSOME WITH TERMINAL P AND Q DELETIONSFINLEY WH; FINLEY SC; TASNEE CHONMAITREE et al.1981; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1981; VOL. 135; NO 8; PP. 729-731; BIBL. 13 REF.Article
SISTER CHROMATID EXCHANGES IN A RING CHROMOSOME 4.BARTRAM CR.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 238-241; BIBL. 13 REF.Article
AN INHERITED TRANSLOCATION T(4;15)(P16;Q22) LEADING TO TWO CASES OF PARTIAL TRISOMY 15COHEN MM; ORNOY A; ROSENMANN A et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 99-103; ABS. FR.; BIBL. 10REF.Article
NEUROPATHOLOGICAL FINDINGS IN WOLF-HIRSCHHORN (4P-) SYNDROMEGOTTFRIED M; LAVINE L; ROESSMANN U et al.1981; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1981; VOL. 55; NO 2; PP. 163-165; BIBL. 15 REF.Article
BRIEF CLINICAL REPORT: PATHOLOGIC FINDINGS IN THE WOLF-HIRSCHHORN (4 P-) SYNDROMEGONZALEZ CH; CAPELOZZI VL; WAJNTAL A et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 3; PP. 183-187; BIBL. 5 REF.Article
NEUROLOGICAL AND NEUROPATHOLOGICAL FINDINGS IN RING CHROMOSOME 4YOUNG RSK; ZALNERAITIS EL.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 6; PP. 487-490; BIBL. 9 REF.Article
MONOSOME HQ 32.1->HQTER SURVENUE DE NOVO CHEZ UN NOUVEAU-NE MULTIMALFORMERETHORE MO; COUTURIER J; MSELATI JC et al.1979; ANN. GENET.; FRA; DA. 1979; VOL. 22; NO 4; PP. 214-216; ABS. ENG; BIBL. 10 REF.Article
ANNEAU DU CHROMOSOME 4. II. SANS DYSMORPHIE FACIALE.CHAVIN COLIN F; TURLEAU C; LIMAL JM et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 2; PP. 105-109; ABS. ANGL.; BIBL. 12 REF.Article