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1
المؤلفون: Suat Caglayan, Sadik Aksit, Halil Aydinlioglu, Bektaşlar D, Cin A, Dizdarer G
المصدر: Scopus-Elsevier
ResearcherIDمصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Hypoplastic genitalia, Hernia, Turkey, Limb Deformities, Congenital, Dwarfism, Short stature, Consanguinity, Frontal Bossing, Genetics, medicine, Humans, Abnormalities, Multiple, Hypertelorism, Genetics (clinical), business.industry, Infant, Newborn, Epigastric hernia, Dysostoses, Genitalia, Female, Syndrome, Toes, medicine.disease, Osteochondrodysplasia, Robinow syndrome, Phenotype, Face, Anteverted nares, Female, Syndactyly, medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::485b2953655a65a004271751bb328c79Test
https://doi.org/10.1111/j.1399-0004.1997.tb02552.xTest -
2
المؤلفون: Z. Kassutto, T. Ben-Ami, S. Kassutto, R. M. Goodman
المصدر: Clinical Genetics. 32:355-359
مصطلحات موضوعية: Adult, Male, Proband, Hearing loss, Hearing Loss, Sensorineural, Nose, Congenital hearing loss, Frontal Bossing, Tongue, Frenulum, otorhinolaryngologic diseases, Genetics, medicine, Humans, Abnormalities, Multiple, Craniofacial, Genetics (clinical), Genes, Dominant, business.industry, Alopecia, Syndrome, Anatomy, Skull, medicine.anatomical_structure, Facial Asymmetry, Child, Preschool, Female, medicine.symptom, business, Facial symmetry
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc9f9b151339146c72ee1492bb6de19bTest
https://doi.org/10.1111/j.1399-0004.1987.tb03301.xTest -
3
المؤلفون: A L Bueno, Joaquín Olivares, Feliciano J. Ramos, O. Bueno, ML Bello, Manuel Bueno
المصدر: Clinical Genetics. 54:400-405
مصطلحات موضوعية: Male, Hearing loss, Osteopathia striata, Frontal Bossing, Genetics, medicine, Humans, Abnormalities, Multiple, Craniofacial, Hypertelorism, Child, Genetics (clinical), Sclerosis, business.industry, Skull, Macrocephaly, Anatomy, medicine.disease, Osteochondrodysplasia, Pedigree, Radiography, medicine.anatomical_structure, Female, Bone Diseases, medicine.symptom, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81be29cb06d7ff544c47314c9b32bfbfTest
https://doi.org/10.1111/j.1399-0004.1998.tb03753.xTest -
4
المؤلفون: Merlin G. Butler, Sarah Hassell
المصدر: Clinical Genetics. 46:372-376
مصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Antley–Bixler syndrome, Anal Canal, Choanal atresia, Nose, Article, Craniosynostosis, Frontal Bossing, Genetics, Exophthalmos, Humans, Medicine, Abnormalities, Multiple, Femur, Genetics (clinical), Respiratory distress, business.industry, Skull, Apnea, Ear, Syndrome, Synostosis, medicine.disease, Hypoplasia, Child, Preschool, Face, Female, medicine.symptom, business, Femoral Fractures
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::037b99f3cae7994f6ec21867f9d33663Test
https://doi.org/10.1111/j.1399-0004.1994.tb04182.xTest -
5
المؤلفون: James V. Higgins, Mary Ella M Pierpont, Michaelene Lopez, Beth A. Conrad, Gordon W. Dewald, Eric R. Christensen
المصدر: Clinical genetics. 48(3)
مصطلحات موضوعية: Genetics, Male, Depressed nasal bridge, Macrocephaly, Infant, Biology, Phenotype, Hypotonia, Frontal Bossing, Terminal (electronics), Chromosomes, Human, Pair 2, Karyotyping, medicine, Humans, Abnormalities, Multiple, medicine.symptom, Chromosome Deletion, Clinical phenotype, Genetics (clinical), Chromosomal Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ba1bb8c8ef7bf67b69c8697ae3aecfeTest
https://pubmed.ncbi.nlm.nih.gov/9184258Test -
6
المؤلفون: L. J. Butler, T. Spencer, W. J. Wall, A. V. Palmer, R. Tabios‐Broadway
المصدر: Clinical genetics. 31(4)
مصطلحات موضوعية: Larynx, Genetic Markers, Sternum, Unusual dermatoglyphics, Epicanthus, Biology, Frontal Bossing, otorhinolaryngologic diseases, Genetics, medicine, Humans, Abnormalities, Multiple, Genetics (clinical), Polydactyly, Skull, Infant, Newborn, Chromosome, Anatomy, medicine.disease, Chromosome Banding, medicine.anatomical_structure, Genetic marker, Female, Chromosome Deletion, Chromosomes, Human, Pair 4, Dermatoglyphics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be7b47db443db8b85c2d93f94a7e7908Test
https://pubmed.ncbi.nlm.nih.gov/3474090Test -
7
المصدر: Clinical genetics. 6(2)
مصطلحات موضوعية: Male, medicine.medical_specialty, Pathology, Encephalopathy, Kidney, Frontal Bossing, Internal medicine, Intellectual Disability, Genetics, Polycystic kidney disease, medicine, Humans, Aspartate Aminotransferases, Hypertelorism, Child, Genetics (clinical), Polycystic Kidney Diseases, L-Lactate Dehydrogenase, business.industry, Liver Diseases, Infant, Alanine Transaminase, Syndrome, medicine.disease, Polycystic kidney, Coloboma, Endocrinology, Liver, Child, Preschool, Karyotyping, Congenital hepatic fibrosis, Female, medicine.symptom, Differential diagnosis, Hepatic fibrosis, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::129f7cea6a10fd02d8bec9dfbcac3ce1Test
https://pubmed.ncbi.nlm.nih.gov/4430157Test -
8
المؤلفون: M. H. K. Shokeir
المصدر: Clinical genetics. 14(3)
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Aneuploidy, Trisomy, Biology, Trisomy 22, Abnormal dermatoglyphics, Paternal Age, Frontal Bossing, Pregnancy, Intellectual Disability, Genetics, medicine, Chromosomes, Human, 21-22 and Y, Humans, Abnormalities, Multiple, Hypertelorism, Child, Genetics (clinical), Epilepsy, medicine.disease, Hypotonia, Chromosome Banding, Pedigree, Abortion, Spontaneous, Palpebral fissure, Female, medicine.symptom, Maternal Age
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e3473c326331b8e16415487787af064Test
https://pubmed.ncbi.nlm.nih.gov/568044Test