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Results: 1-11 |
Results: 11
AUTISM AND MATERNALLY DERIVED ABERRATIONS OF CHROMOSOME 15Q
Authors: SCHROER RJ PHELAN MC MICHAELIS RC CRAWFORD EC SKINNER SA CUCCARO M SIMENSEN RJ BISHOP J SKINNER C FENDER D STEVENSON RE
Citation: Rj. Schroer et al., AUTISM AND MATERNALLY DERIVED ABERRATIONS OF CHROMOSOME 15Q, American journal of medical genetics, 76(4), 1998, pp. 327-336
INTERSITIAL DELETION OF 20P - NEW CANDIDATE REGION FOR HIRSCHSPRUNG-DISEASE AND AUTISM
Authors: MICHAELIS RC SKINNER SA DEASON R SKINNER C MOORE CL PHELAN MC
Citation: Rc. Michaelis et al., INTERSITIAL DELETION OF 20P - NEW CANDIDATE REGION FOR HIRSCHSPRUNG-DISEASE AND AUTISM, American journal of medical genetics, 71(3), 1997, pp. 298-304
GIANT OF A FORMER AGE - A FINAL NOTE ON BOONE,JAMES,SHERGOLD
Authors: SKINNER SA
Citation: Sa. Skinner, GIANT OF A FORMER AGE - A FINAL NOTE ON BOONE,JAMES,SHERGOLD, Notes and queries, 44(3), 1997, pp. 336-338
TRINUCLEOTIDE REPEAT EXPANSIONS IN THE FMR1 AND FMR2 GENES ARE NOT COMMON ETIOLOGIC FACTORS IN AUTISTIC-CHILDREN
Authors: LONGSHORE JW TARLETON JC SCHWARTZ CE SKINNER C SKINNER SA SCHROER RJ STEVENSON RE
Citation: Jw. Longshore et al., TRINUCLEOTIDE REPEAT EXPANSIONS IN THE FMR1 AND FMR2 GENES ARE NOT COMMON ETIOLOGIC FACTORS IN AUTISTIC-CHILDREN, American journal of human genetics, 61(4), 1997, pp. 592-592
THE MICROVASCULAR STRUCTURE OF THE NORMAL COLON IN RATS AND HUMANS
Authors: SKINNER SA OBRIEN PE
Citation: Sa. Skinner et Pe. Obrien, THE MICROVASCULAR STRUCTURE OF THE NORMAL COLON IN RATS AND HUMANS, The Journal of surgical research, 61(2), 1996, pp. 482-490
DELETION OF 15Q11-]Q13 IN A MOTHER AND SON WITHOUT FEATURES OF PRADER-WILLI OR ANGELMAN SYNDROME
Authors: PHELAN MC MICHAELIS RC TARLETON JC DONLON TA SKINNER SA
Citation: Mc. Phelan et al., DELETION OF 15Q11-]Q13 IN A MOTHER AND SON WITHOUT FEATURES OF PRADER-WILLI OR ANGELMAN SYNDROME, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 116-116
PRENATAL-DIAGNOSIS OF MOSAIC 4P - IN A FETUS WITH TRISOMY-21
Authors: PHELAN MC SAUL RA GAILEY TA SKINNER SA
Citation: Mc. Phelan et al., PRENATAL-DIAGNOSIS OF MOSAIC 4P - IN A FETUS WITH TRISOMY-21, Prenatal diagnosis, 15(3), 1995, pp. 274-277
MICROVASCULAR STRUCTURE OF BENIGN AND MALIGNANT-TUMORS OF THE COLON IN HUMANS
Authors: SKINNER SA FRYDMAN GM OBRIEN PE
Citation: Sa. Skinner et al., MICROVASCULAR STRUCTURE OF BENIGN AND MALIGNANT-TUMORS OF THE COLON IN HUMANS, Digestive diseases and sciences, 40(2), 1995, pp. 373-384
DELETION INVOLVING D15S113 IN A MOTHER AND SON WITHOUT ANGELMAN-SYNDROME - REFINEMENT OF THE ANGELMAN-SYNDROME CRITICAL DELETION REGION
Authors: MICHAELIS RC SKINNER SA LETHCO BA SIMENSEN RJ DONLON TA TARLETON J PHELAN MC
Citation: Rc. Michaelis et al., DELETION INVOLVING D15S113 IN A MOTHER AND SON WITHOUT ANGELMAN-SYNDROME - REFINEMENT OF THE ANGELMAN-SYNDROME CRITICAL DELETION REGION, American journal of medical genetics, 55(1), 1995, pp. 120-126
LAPAROSCOPIC ASSISTED RIGHT HEMICOLECTOMY WITH VALTRAC BAR (BIOFRAGMENTABLE ANASTOMOTIC RING) ILEOTRANSVERSE ANASTOMOSIS
Authors: POLGLASE AL SKINNER SA JOHNSON WR
Citation: Al. Polglase et al., LAPAROSCOPIC ASSISTED RIGHT HEMICOLECTOMY WITH VALTRAC BAR (BIOFRAGMENTABLE ANASTOMOTIC RING) ILEOTRANSVERSE ANASTOMOSIS, Australian and New Zealand journal of surgery, 63(6), 1993, pp. 481-484
THE PROTEUS FOOT - A PATHOGNOMONIC SIGN
Authors: SAUL RA SKINNER SA BOYD E STEVENSON RE
Citation: Ra. Saul et al., THE PROTEUS FOOT - A PATHOGNOMONIC SIGN, American journal of human genetics, 53(3), 1993, pp. 501-501
Risultati: 1-11 |