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Results: 1-8 |
Results: 8
HETEROALLELIC MONOZYGOTIC TWINS AND TRIPLETS
Authors: CANTU JM DIAZGALLARDO MY BARROSNUNEZ P FIGUERA LE
Citation: Jm. Cantu et al., HETEROALLELIC MONOZYGOTIC TWINS AND TRIPLETS, American journal of medical genetics, 77(2), 1998, pp. 166-167
HIGH RECURRENCE OF RECOMBINANTS IN A FAMILY WITH PERICENTRIC-INVERSION OF CHROMOSOME-18
Authors: MEJIABALTODANO G BOBADILLA L GONZALEZ RM BARROSNUNEZ P
Citation: G. Mejiabaltodano et al., HIGH RECURRENCE OF RECOMBINANTS IN A FAMILY WITH PERICENTRIC-INVERSION OF CHROMOSOME-18, Annales de genetique, 40(3), 1997, pp. 164-168
RECESSIVE SCHWARTZ-JAMPEL SYNDROME (SJS) - CONFIRMATION OF LINKAGE TOCHROMOSOME 1P, EVIDENCE OF GENETIC HOMOGENEITY AND REDUCTION OF THE SJS LOCUS TO A 3-CM INTERVAL
Authors: FONTAINE B NICOLE S TOPALOGLU H BENHAMIDA C BEIGHTON P SPAANS F CANTU JMA BAKOURI S ROMERO N RICKER K BARROSNUNEZ P PONSOT G BENHAMIDA M WEISSENBACH J HENTATI F LEHMANNHORN F
Citation: B. Fontaine et al., RECESSIVE SCHWARTZ-JAMPEL SYNDROME (SJS) - CONFIRMATION OF LINKAGE TOCHROMOSOME 1P, EVIDENCE OF GENETIC HOMOGENEITY AND REDUCTION OF THE SJS LOCUS TO A 3-CM INTERVAL, Human genetics, 98(3), 1996, pp. 380-385
MOLECULAR CHARACTERIZATION OF THE FRAGILE-X SYNDROME IN THE MEXICAN POPULATION
Authors: DIAZGALLARDO MY BARROSNUNEZ P DIAZ CA HERNANDEZ A GOMEZESPINEL I LEAL CA FRAGOSO R FIGUERA L GARCIACRUZ D RAMIREZDUENAS ML CANTU JM
Citation: My. Diazgallardo et al., MOLECULAR CHARACTERIZATION OF THE FRAGILE-X SYNDROME IN THE MEXICAN POPULATION, Archives of medical research, 26, 1995, pp. 77-83
GENETIC AND CONGENITAL DISEASES IN A MEXICAN PEDIATRIC-HOSPITAL
Authors: BARROSNUNEZ P MEDINA C
Citation: P. Barrosnunez et C. Medina, GENETIC AND CONGENITAL DISEASES IN A MEXICAN PEDIATRIC-HOSPITAL, Brazilian journal of genetics, 18(3), 1995, pp. 451-457
UNEXPECTED FAMILIAL RECURRENCE OF IRIS COLOBOMA - A DELAYED MUTATION MECHANISM
Authors: BARROSNUNEZ P MEDINA C MENDOZA R SANCHEZCORONA J GARCIACRUZ D
Citation: P. Barrosnunez et al., UNEXPECTED FAMILIAL RECURRENCE OF IRIS COLOBOMA - A DELAYED MUTATION MECHANISM, Clinical genetics, 48(3), 1995, pp. 160-161
PATERNAL NONDISJUNCTION EVIDENCED BY G6PD ELECTROPHORETIC PHENOTYPES IN A 48,XXXY PATIENT
Authors: MEDINA C ZUNIGA G RAMIREZ G RIVERA H FRANCOGAMBOA E BARROSNUNEZ P VACA G
Citation: C. Medina et al., PATERNAL NONDISJUNCTION EVIDENCED BY G6PD ELECTROPHORETIC PHENOTYPES IN A 48,XXXY PATIENT, Annales de genetique, 37(1), 1994, pp. 37-38
TRANSLOCATION 43 WITH ADJACENT 1 AND 3-1 SEGREGATIONS LEADING TO COMPLEMENTARY SEGMENTAL TRISOMIES 13
Authors: BARROSNUNEZ P HIGAREDA O CANTU JM
Citation: P. Barrosnunez et al., TRANSLOCATION 43 WITH ADJACENT 1 AND 3-1 SEGREGATIONS LEADING TO COMPLEMENTARY SEGMENTAL TRISOMIES 13, Annales de genetique, 36(3), 1993, pp. 176-180
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