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47, XY, T(9P+; 11Q+) IN A MALE INFANT WITH MULTIPLE MALFORMATIONS = , XY, T (9P+; 11Q+) CHEZ UN NOURRISSON MALE POLYMALFORMEDINNO ND; SILVEY GL; WEISSKOPF B et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 2; PP. 125-131; BIBL. 11REF.Article

THE 9P-DELETION SYNDROME. REPORT OF A PATIENT WITH A 46,XX,9P-CONSTITUTION DUE TO A PATERNAL T(9P-;15Q+) TRANSLOCATIONORYE E; VERHAAREN H; VAN DEN BOAERT VAN HEESVELDE AM et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 349-357; BIBL. 8 REF.Article

A CASE OF (9P+,13Q-) TRANSLOCATION. CYTOGENETICS AND FAMILY HISTORYJOTTERAND M; CATTI A; JUILLARD E et al.1975; ARCH. GENET.; SCHWEIZ; DA. 1975; VOL. 48; NO 1; PP. 75; (SCHWEIZ. GES. GENET. JAHRESVERSAMML. ZUSAMMENFASSUNGEN REFRATE; LAUSANNE; 1974)Conference Paper

TRISOMY 9 P AND UNUSUAL TRANSLOCATION MONGOLISM IN SIBLINGS DUE TO DIFFERENT 3: 1 SEGREGATIONS OF MATERNAL TRANSLOCATION RCP (9:21)(P11; Q11).HABEDANK M; FAUST J.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 251-256; BIBL. 15 REF.Article

FAMILIAL C/D TRANSLOCATION T(9;13) (9P23; 13Q21) IN A MALE ASSOCIATED WITH RECURRENT ABORTION.PAL SINGH KAHLON D; SERRA A.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 223-230; BIBL. 1 P. 1/2Article

A NEW CASE OF TRISOMY FOR THE DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9;13) (P21;Q21).JOTTERAND M; JUILLARD E.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 213-222; BIBL. 20 REF.Article

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