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Results: 1-25 | 26-33 |
Results: 26-33/33
DE-NOVO DIRECT DUPLICATION 7P(P11.2-]PTER) IN AN ARAB CHILD WITH MCA MR SYNDROME - TRISOMY 7P A DELINEATED SYNDROME/
Authors: REDHA MA MURTHY DSK ALAWADI SA ALSULAIMAN IS SABRY MA ELBAHEY SA FARAG TI
Citation: Ma. Redha et al., DE-NOVO DIRECT DUPLICATION 7P(P11.2-]PTER) IN AN ARAB CHILD WITH MCA MR SYNDROME - TRISOMY 7P A DELINEATED SYNDROME/, Annales de genetique, 39(1), 1996, pp. 5-9
RIGHT UPPER-LIMB BUD TRIPLICATION AND POLYTHELIA, LEFT-SIDED HEMIHYPERTROPHY AND CONGENITAL HIP DISLOCATION, FACIAL DYSMORPHISM, CONGENITALHEART-DISEASE, AND SCOLIOSIS - DISORGANIZATION-LIKE SPECTRUM OR PATTERNING GENE DEFECT
Authors: SABRY MA ALSALEH Q ALSAWAN R ALAWADI SA FARAG TI
Citation: Ma. Sabry et al., RIGHT UPPER-LIMB BUD TRIPLICATION AND POLYTHELIA, LEFT-SIDED HEMIHYPERTROPHY AND CONGENITAL HIP DISLOCATION, FACIAL DYSMORPHISM, CONGENITALHEART-DISEASE, AND SCOLIOSIS - DISORGANIZATION-LIKE SPECTRUM OR PATTERNING GENE DEFECT, Journal of Medical Genetics, 32(7), 1995, pp. 555-556
DE-NOVO DIRECT DUPLICATION 7P(P11.3-]PTER) IN AN ARAB CHILD WITH MCA MR SYNDROME - TRISOMY-7P A DELINEATED CHROMOSOMAL SYNDROME/
Authors: REDHA MA MURTHY DSK ALAWADI SA ALSULAIMAN IS SABRY MA ELBAHEY SA FARAG FI
Citation: Ma. Redha et al., DE-NOVO DIRECT DUPLICATION 7P(P11.3-]PTER) IN AN ARAB CHILD WITH MCA MR SYNDROME - TRISOMY-7P A DELINEATED CHROMOSOMAL SYNDROME/, American journal of human genetics, 57(4), 1995, pp. 661-661
A POSSIBLE NEW VARIANT OF NONSYNDROMIC LISSENCEPHALY, ASSOCIATED WITHMYOCLONIC EPILEPSY
Authors: FARAH S RUDWAN M KHAFAGI S KHURAIBET A QASRAWI B ALBUSAIRI W HASSAN M HASSEEB N ELGAMAL SA SABRY MA FARAG TI
Citation: S. Farah et al., A POSSIBLE NEW VARIANT OF NONSYNDROMIC LISSENCEPHALY, ASSOCIATED WITHMYOCLONIC EPILEPSY, American journal of human genetics, 57(4), 1995, pp. 1773-1773
A POSSIBLE NEW CRANIO FACIO FRONTO DIGITAL DYSPLASIA
Authors: QASRAWI BM ELGAMAL SA FARAG TI ALAWADI SA ALGENDI II SABRY MA
Citation: Bm. Qasrawi et al., A POSSIBLE NEW CRANIO FACIO FRONTO DIGITAL DYSPLASIA, American journal of human genetics, 57(4), 1995, pp. 1778-1778
A POSSIBLE NEW SYNDROMIC SITUS-INVERSUS TOTALIS IN AN INSTITUTIONALIZED PATIENT
Authors: SABRY MA MUBASHIR MA HASSEEB N ALAWADI SA FARAH SA QASRAWI B ALDABBOUS RM ALBUSAIRI W FARAG TI
Citation: Ma. Sabry et al., A POSSIBLE NEW SYNDROMIC SITUS-INVERSUS TOTALIS IN AN INSTITUTIONALIZED PATIENT, American journal of human genetics, 57(4), 1995, pp. 1782-1782
POSSIBLE GENETIC-HETEROGENEITY IN THE ROBERTS-SC PHOCOMELIA SYNDROME
Authors: SABRY MA
Citation: Ma. Sabry, POSSIBLE GENETIC-HETEROGENEITY IN THE ROBERTS-SC PHOCOMELIA SYNDROME, Human heredity, 45(4), 1995, pp. 241-242
THE POSSIBLE MIDDLE-EAST ORIGIN OF THE MUTATION FOR THE LIMB PELVIS HYPOPLASIA/APLASIA SYNDROME/
Authors: SABRY MA
Citation: Ma. Sabry, THE POSSIBLE MIDDLE-EAST ORIGIN OF THE MUTATION FOR THE LIMB PELVIS HYPOPLASIA/APLASIA SYNDROME/, Journal of Medical Genetics, 31(11), 1994, pp. 897-897
Risultati: 1-25 | 26-33 |