| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/S0344-0338(97)80018-0 |
| P698 | PubMed publication ID | 9406252 |
| P2093 | author name string | Stein H | |
| Otto HF | |||
| Sergi C | |||
| Heep JG | |||
| P2860 | cites work | A new acro-cranio-facial dysostosis syndrome in sisters | Q56404138 |
| Brief clinical report: a sixth report (eighth case) of craniosynostosis-radial aplasia (Baller-Gerold) syndrome | Q56417981 | ||
| Demographic, reproductive, medical, and environmental factors in relation to gastroschisis | Q60727551 | ||
| Germinal mosaicism in Crouzon syndrome | Q68323852 | ||
| Exophthalmus--prenatal ultrasonic features for diagnosis of Crouzon syndrome | Q69566978 | ||
| Young maternal age and smoking during pregnancy as risk factors for gastroschisis | Q70664966 | ||
| Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome | Q24310222 | ||
| Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2 | Q24315050 | ||
| Dubowitz syndrome: possible evidence for a clinical subtype | Q28246042 | ||
| A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis | Q28249477 | ||
| Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome) | Q28261864 | ||
| An autosomal recessive form of craniofacial dysostosis (the Crouzon syndrome). | Q33585584 | ||
| Craniosynostosis and lid anomalies: report of a girl with Michels syndrome | Q34259643 | ||
| Trigonocephaly: a new familial syndrome | Q34267874 | ||
| Antley-Bixler syndrome in sisters: a term newborn and a prenatally diagnosed fetus | Q34271081 | ||
| Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans | Q34289809 | ||
| Classification of previously unclassified cases of craniosynostosis | Q34414601 | ||
| Holoprosencephaly and primary craniosynostosis: the Genoa syndrome | Q34729181 | ||
| Contribution of Demographic and Environmental Factors to the Etiology of Gastroschisis: A Hypothesis | Q37122258 | ||
| Monozygotic twins discordant for gastroschisis: case report and review of the literature of twins and familial occurrence of gastroschisis | Q40557058 | ||
| Antley-Bixler syndrome: report of a patient and review of literature. | Q40612463 | ||
| Hypomandibular faciocranial dysostosis: another case and review | Q40728756 | ||
| Further delineation of the Baller-Gerold syndrome | Q40893454 | ||
| Studies of malformation syndromes of man XXXIX: a craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: "craniofacial dyssynostosis". | Q41060006 | ||
| First trimester maternal medication use in relation to gastroschisis | Q41112233 | ||
| Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods | Q44208349 | ||
| Genetic-epidemiologic study of omphalocele and gastroschisis: evidence for heterogeneity | Q44483352 | ||
| A heritable syndrome of craniosynostosis, short thin hair, dental abnormalities, and short limbs: cranioectodermal dysplasia | Q44931195 | ||
| C syndrome with apparently normal development | Q46787158 | ||
| Omphalocele and gastroschisis in Europe: a survey of 3 million births 1980-1990. EUROCAT Working Group. | Q51047552 | ||
| Early operation in craniofacial dysostosis. | Q51751300 | ||
| Craniosynostosis and kidney malformation in a case of Hennekam syndrome. | Q52016259 | ||
| Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. | Q52034036 | ||
| Craniosynostosis-radial aplasia syndrome | Q52317325 | ||
| Lambdoid synostosis is an overdiagnosed condition | Q56384154 | ||
| Resorbable coupling fixation in craniosynostosis surgery: experimental and clinical applications | Q56384298 | ||
| Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture | Q56384329 | ||
| Craniomicromelic syndrome: a newly recognized lethal condition with craniosynostosis, distinct facial anomalies, short limbs, and intrauterine growth retardation | Q56384343 | ||
| P433 | issue | 8 | |
| P921 | main subject | craniosynostosis | Q378183 |
| renal agenesis | Q669435 | ||
| gastroschisis | Q1495674 | ||
| P304 | page(s) | 579-85; discussion 587-8 | |
| P577 | publication date | 1997-01-01 | |
| P1433 | published in | Pathology, Research and Practice | Q15758752 |
| P1476 | title | A 19-week-old fetus with craniosynostosis, renal agenesis and gastroschisis: case report and differential diagnosis | |
| P478 | volume | 193 |
| Q36601109 | Fibroblast growth factor receptor signaling in kidney and lower urinary tract development. |
| Q56357898 | Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis |
| Q33556357 | Role of fibroblast growth factor receptor signaling in kidney development |
| Q80167720 | Role of fibroblast growth factor receptor signaling in kidney development |
| Q84196885 | Role of fibroblast growth factor receptor signaling in kidney development |
Search more.