ACNP - Italian Periodicals Catalogue

AAAAAA

ITA
ENG

Results: 1-10 |

Results: 10

NEUROFIBROMATOSIS - A COMMON NEUROCUTANEOUS DISORDER

Authors: KARNES PS

Citation: Ps. Karnes, NEUROFIBROMATOSIS - A COMMON NEUROCUTANEOUS DISORDER, Mayo Clinic proceedings, 73(11), 1998, pp. 1071-1076

GENE-SPECIFIC INFLUENCE ON THE TRIGGERS FOR CARDIAC-ARREST IN THE LONG QT SYNDROME

Authors: SCHWARTZ PJ MOSS AJ PRIORI SG WANG Q LEHMANN MH TIMOTHY K DENJOY IF HAVERKAMP W GUICHENEY P PAGANINI V SCHEINMAN MM KARNES PS

Citation: Pj. Schwartz et al., GENE-SPECIFIC INFLUENCE ON THE TRIGGERS FOR CARDIAC-ARREST IN THE LONG QT SYNDROME, Circulation, 96(8), 1997, pp. 1170-1170

FAMILIAL RECURRENCE OF TRACHEOESOPHAGEAL FISTULA AND ASSOCIATED MALFORMATIONS

Authors: MCMULLEN KP KARNES PS MOIR CR MICHELS VV

Citation: Kp. Mcmullen et al., FAMILIAL RECURRENCE OF TRACHEOESOPHAGEAL FISTULA AND ASSOCIATED MALFORMATIONS, American journal of medical genetics, 63(4), 1996, pp. 525-528

ORDERING AND INTERPRETING DNA TESTS

Authors: KARNES PS

Citation: Ps. Karnes, ORDERING AND INTERPRETING DNA TESTS, Mayo Clinic proceedings, 71(12), 1996, pp. 1192-1195

CYTOGENETIC TESTING FOR WILLIAMS-SYNDROME

Authors: JALAL SM CRIFASI PA KARNES PS MICHELS VV

Citation: Sm. Jalal et al., CYTOGENETIC TESTING FOR WILLIAMS-SYNDROME, Mayo Clinic proceedings, 71(1), 1996, pp. 67-68

UNIPARENTAL DISOMY IN CONGENITAL DISORDERS - A PROSPECTIVE-STUDY

Authors: LINDOR NM KARNES PS MICHELS VV DEWALD GW GOERSS J JALAL S JENKINS RB VOCKLEY G THIBODEAU SN

Citation: Nm. Lindor et al., UNIPARENTAL DISOMY IN CONGENITAL DISORDERS - A PROSPECTIVE-STUDY, American journal of medical genetics, 58(2), 1995, pp. 143-146

LABORATORY MEDICINE AND PATHOLOGY - INITIAL ASSESSMENT OF INFANTS ANDCHILDREN WITH SUSPECTED INBORN-ERRORS OF METABOLISM

Authors: LINDOR NM KARNES PS

Citation: Nm. Lindor et Ps. Karnes, LABORATORY MEDICINE AND PATHOLOGY - INITIAL ASSESSMENT OF INFANTS ANDCHILDREN WITH SUSPECTED INBORN-ERRORS OF METABOLISM, Mayo Clinic proceedings, 70(10), 1995, pp. 987-988

SYMPTOMATIC PORTAL-HYPERTENSION IN DYSKERATOSIS-CONGENITA - MAYO-CLINIC EXPERIENCE AND REVIEW OF THE LITERATURE

Authors: ZEMBOWER TR CHAREONTHAITAWEE P KARNES PS NAGORNEY DM CARPENTER HA DOUGLAS DD PHYLIKY RL GROSS JB

Citation: Tr. Zembower et al., SYMPTOMATIC PORTAL-HYPERTENSION IN DYSKERATOSIS-CONGENITA - MAYO-CLINIC EXPERIENCE AND REVIEW OF THE LITERATURE, Gastroenterology, 108(4), 1995, pp. 1209-1209

MOSAIC TRISOMY-16 IN A THRIVING INFANT - MATERNAL HETERODISOMY FOR CHROMOSOME-16

Authors: LINDOR NM JALAL SM THIBODEAU SN BONDE D SAUSER KL KARNES PS

Citation: Nm. Lindor et al., MOSAIC TRISOMY-16 IN A THRIVING INFANT - MATERNAL HETERODISOMY FOR CHROMOSOME-16, Clinical genetics, 44(4), 1993, pp. 185-189

CYTOGENETIC AND MOLECULAR STUDIES OF A DUPLICATION OF XQ26 AND XQ27 IN 2 BROTHERS WITH NEURAL-TUBE DEFECTS

Authors: GOERSS JB KARNES PS THIBODEAU SN JOHNSON DD ZIMMERMAN D DEWALD GW

Citation: Jb. Goerss et al., CYTOGENETIC AND MOLECULAR STUDIES OF A DUPLICATION OF XQ26 AND XQ27 IN 2 BROTHERS WITH NEURAL-TUBE DEFECTS, American journal of human genetics, 53(3), 1993, pp. 440-440

Risultati: 1-10 |