AAAAAA

   
Results: 1-7 |
Results: 7
DETECTION OF A CONCOMITANT DISTAL DELETION IN AN INVERTED DUPLICATIONOF CHROMOSOME-3 - IS THERE AN OVERALL MECHANISM FOR THE ORIGIN OF SUCH DUPLICATIONS DEFICIENCIES/
Authors: JENDERNY J POETSCH M HOELTZENBEIN M FRIEDRICH U JAUCH A
Citation: J. Jenderny et al., DETECTION OF A CONCOMITANT DISTAL DELETION IN AN INVERTED DUPLICATIONOF CHROMOSOME-3 - IS THERE AN OVERALL MECHANISM FOR THE ORIGIN OF SUCH DUPLICATIONS DEFICIENCIES/, European journal of human genetics, 6(5), 1998, pp. 439-444
PRESENCE OF THE AZF REGION IN A FEMALE WITH AN IDIC(Y)(Q11)
Authors: JENDERNY J SCHMIDT W HELD KR
Citation: J. Jenderny et al., PRESENCE OF THE AZF REGION IN A FEMALE WITH AN IDIC(Y)(Q11), Clinical genetics, 54(4), 1998, pp. 341-344
MILD PHENOTYPIC MANIFESTATIONS OF TERMINAL DELETION OF THE LONG ARM OF CHROMOSOME-4 - CLINICAL DESCRIPTION OF A NEW PATIENT
Authors: CALIEBE A WALTZ S JENDERNY J
Citation: A. Caliebe et al., MILD PHENOTYPIC MANIFESTATIONS OF TERMINAL DELETION OF THE LONG ARM OF CHROMOSOME-4 - CLINICAL DESCRIPTION OF A NEW PATIENT, Clinical genetics, 52(2), 1997, pp. 116-119
INTERPHASE CYTOGENETICS ON PARAFFIN SECTIONS OF PEDIATRIC EXTRAGONADAL YOLK-SAC TUMORS
Authors: JENDERNY J KOSTER E BORCHERS O MEYER A GROTE W HARMS D JANIG U
Citation: J. Jenderny et al., INTERPHASE CYTOGENETICS ON PARAFFIN SECTIONS OF PEDIATRIC EXTRAGONADAL YOLK-SAC TUMORS, Virchows Archiv, 428(1), 1996, pp. 53-57
DETECTION OF CHROMOSOME-ABERRATIONS IN PARAFFIN SECTIONS OF 7 GONADALYOLK-SAC TUMORS OF CHILDHOOD
Authors: JENDERNY J KOSTER E MEYER A BORCHERS O GROTE W HARMS D JANIG U
Citation: J. Jenderny et al., DETECTION OF CHROMOSOME-ABERRATIONS IN PARAFFIN SECTIONS OF 7 GONADALYOLK-SAC TUMORS OF CHILDHOOD, Human genetics, 96(6), 1995, pp. 644-650
TRANSMISSION OF A RING CHROMOSOME-18 FROM A MOTHER WITH 46,XX 47,XX,+R(18) MOSAICISM TO HER DAUGHTER, RESULTING IN A 46,XX,R(18) KARYOTYPE/
Authors: JENDERNY J CALIEBE A BEYER C GROTE W
Citation: J. Jenderny et al., TRANSMISSION OF A RING CHROMOSOME-18 FROM A MOTHER WITH 46,XX 47,XX,+R(18) MOSAICISM TO HER DAUGHTER, RESULTING IN A 46,XX,R(18) KARYOTYPE/, Journal of Medical Genetics, 30(11), 1993, pp. 964-965
ANALYSIS OF A TERMINAL XP22.3 DELETION IN A PATIENT WITH 6 MONOGENIC DISORDERS - IMPLICATIONS FOR THE MAPPING OF X-LINKED OCULAR ALBINISM
Authors: MEINDL A HOSENFELD D BRUCKL W SCHUFFENHAUER S JENDERNY J BACSKULIN A OPPERMANN HC SWENSSON O BOULOUX P MEITINGER T
Citation: A. Meindl et al., ANALYSIS OF A TERMINAL XP22.3 DELETION IN A PATIENT WITH 6 MONOGENIC DISORDERS - IMPLICATIONS FOR THE MAPPING OF X-LINKED OCULAR ALBINISM, Journal of Medical Genetics, 30(10), 1993, pp. 838-842
Risultati: 1-7 |