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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Gene Spectrum and Clinica" (30 stories)

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Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS–FTD spectrum
Lead StoryNaturegeneral
May 19

Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS–FTD spectrum

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9DVFlXaFVIS05HUW05MXRlX0k2RmVob0ttdEYxelFDbWhNSlN5T0t0c3Y2YnpXWW9lYjRCaTB3MURKMDRHNkhQSlJybVdRR3hzT2dLbndycV81YWRlRUFn?oc=5" target="_blank">Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS–FTD spectrum</a>  <font color="#6f6f6f">Nature</font>

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Search Results for "Gene Spectrum and Clinica"

Updated every 3 minutes via FreeNewsApi, GNews, Currents API & Google News

29 stories displayed
Autism Spectrum Disorder (ASD) Symptoms & Causes
Cleveland Clinicgeneral

Autism Spectrum Disorder (ASD) Symptoms & Causes

<a href="https://news.google.com/rss/articles/CBMiY0FVX3lxTE5YdF8zazBlU091VlRUajFkWmZtd3Y4SVYzRW9fMWZ4QTYwUURVSkRZV3RqT08wX2g0ZDl6ckNSdDVZdHJDaXcwMGs0OHA3SmtMMnNxbi1QejI2aHVwSVdHNzlUcw?oc=5" target="_blank">Autism Spectrum Disorder (ASD) Symptoms & Causes</a>  <font color="#6f6f6f">Cleveland Clinic</font>

'Superheroes' at a Bay Area company just launched the first clinical trial in an autism spectrum disorder — 'Our ultimate goal is a cure'
The Business Journalsworld

'Superheroes' at a Bay Area company just launched the first clinical trial in an autism spectrum disorder — 'Our ultimate goal is a cure'

<a href="https://news.google.com/rss/articles/CBMirwFBVV95cUxQUWpKWk9hTmEzX1cxeGQwajdqWnBmZG1IWERZZEVzeXZ5U1FCS3B4Rk1FdUxsMkxyQXdsc3ZBMjZ0V0xha19wcW04V0RKOFh2dzBjcFEzVkMwVTA0MjlIRFdsZTdlbjFCbEVleFhmR0p3cGYxcGNYT0tEMUNqX0g4MkhwUW4wS053Z2FDMG5sS1FJUFpuRmtMaTN0Z3EzSmJ5TDdHY2Q0bHVBSjM4OXZ3?oc=5" target="_blank">'Superheroes' at a Bay Area company just launched the first clinical trial in an autism spectrum disorder — 'Our ultimate goal is a cure'</a>  <font color="#6f6f6f">The Business Journals</font>

Gene Spectrum and Clinical Traits of Nine Patients With Oocyte Maturation Arrest
Frontierstech

Gene Spectrum and Clinical Traits of Nine Patients With Oocyte Maturation Arrest

<a href="https://news.google.com/rss/articles/CBMijgFBVV95cUxPMlhTaDg2Nm9CLWZ6MVZHWU5IZTkyZFp6aFdyNHJ3RUFqNGZ0ZWJoZEwwdU9IZkNYNHczM05xSzdDSk1nZm9hWGNJYjlCd3hTdU5vU25IME9jVzljNFNSTFBRc0MwaHRtOGpiSzhReDd1OWk1X245YjZsd0VWUDZoQVFkcTlkNWU0ck1kRDBR?oc=5" target="_blank">Gene Spectrum and Clinical Traits of Nine Patients With Oocyte Maturation Arrest</a>  <font color="#6f6f6f">Frontiers</font>

Clinical and genomic features of Lynch syndrome differ by tumor site and disease spectrum
Naturegeneral

Clinical and genomic features of Lynch syndrome differ by tumor site and disease spectrum

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1sVy11NWN3UndIZUU1SFRBUnZaUDVtTWo4ZmxmMnNLX2s3ckRjOG5iOWZRYzFjd2NaQnlkZlU4Tlh3SGNpVkhqeTk5Ml8tdHhNOWJiakxRVzJLMTc4eDFJ?oc=5" target="_blank">Clinical and genomic features of Lynch syndrome differ by tumor site and disease spectrum</a>  <font color="#6f6f6f">Nature</font>

Clinical Spectrum of Obesity and Mutations in the Melanocortin 4 Receptor Gene
NEJMgeneral

Clinical Spectrum of Obesity and Mutations in the Melanocortin 4 Receptor Gene

<a href="https://news.google.com/rss/articles/CBMiXkFVX3lxTE9VMXBSZC1GX0w3M2ttTkRkamdtdWlsLWFiSFV1NUFiMlpqRUc1NUl4el9NX29pU0t0c1ZiSEF0OER3M0lnNlZKODF0cEc3V1EwYzNOWWpDQ1lWMFBfNlE?oc=5" target="_blank">Clinical Spectrum of Obesity and Mutations in the Melanocortin 4 Receptor Gene</a>  <font color="#6f6f6f">NEJM</font>

Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia Syndromes
American Heart Association Journalsgeneral

Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia Syndromes

<a href="https://news.google.com/rss/articles/CBMiakFVX3lxTE1YQWlwX2hhVTBDbXFoaEJUdjV0NDR4ZDFZa1NKSG1iT3VSbjVJTlpXR05STkhKUXNnd1dteFhOYXA0a1ZXV3VMRXFFN2dBVWg5ZnNSaEp2VnhxeFQwdnZaOFdzbG1PMUQ5YkE?oc=5" target="_blank">Spectrum of Mutations and Long-Term Clinical Outcomes in Genetic Chylomicronemia Syndromes</a>  <font color="#6f6f6f">American Heart Association Journals</font>

Expanded clinical, genetic, and biological spectrum of filaminopathies with hematological involvement
Haematologicageneral

Expanded clinical, genetic, and biological spectrum of filaminopathies with hematological involvement

<a href="https://news.google.com/rss/articles/CBMiV0FVX3lxTE5zempDY3NsWXUxbmtFbl9PNG93U0QxckNEUFBwM1R0UXlRbTV2Q1dlRTItTXVrd2d6OERnWUVIUjVhWEJ0cGJtM3NkVFVJXzVTVmlNOXBhMA?oc=5" target="_blank">Expanded clinical, genetic, and biological spectrum of filaminopathies with hematological involvement</a>  <font color="#6f6f6f">Haematologica</font>

Targeted sequencing and clinical strategies in children with autism spectrum disorder: A cohort study
Frontiersgeneral

Targeted sequencing and clinical strategies in children with autism spectrum disorder: A cohort study

<a href="https://news.google.com/rss/articles/CBMijwFBVV95cUxQTVU3SVh4dW11RVp5Nk4zcHVMdWJwdldfcHBuZUstYlZZRTd2VEFpRDNOcng1MWRwdFV1QzF2elJZZnlabUhnZUozS2owZ2tzWHpnd2lKMzc5UDJxbTNzOUFVLTFINjNNVzIybHN1ZUs3c0dyQnAxTnZsN1FCbE1PU0xQSURxUW9PaHRxQmlyWQ?oc=5" target="_blank">Targeted sequencing and clinical strategies in children with autism spectrum disorder: A cohort study</a>  <font color="#6f6f6f">Frontiers</font>

Expanding genetic and clinical spectra of β-tubulinopathies: A Korean study | Journal of Human Genetics
Naturegeneral

Expanding genetic and clinical spectra of β-tubulinopathies: A Korean study | Journal of Human Genetics

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE41RUNCREgyb3BTMGduRWR1enRoRTJFUFRINWVlMUpFT1F3dkFQdVRra0pscGRGOFoxaGdmMzRpZ2FDMUpCcEduSFowLTJoQW5FRGs3TC1qX0ltWUVHZWJN?oc=5" target="_blank">Expanding genetic and clinical spectra of β-tubulinopathies: A Korean study | Journal of Human Genetics</a>  <font color="#6f6f6f">Nature</font>

Clinical and mutational spectrum of paediatric Charcot-Marie-Tooth disease in a large cohort of Chinese patients
Frontiersgeneral

Clinical and mutational spectrum of paediatric Charcot-Marie-Tooth disease in a large cohort of Chinese patients

<a href="https://news.google.com/rss/articles/CBMijwFBVV95cUxNYm9SRlhKaWdvSm1iOGpLZUUtd2xGNTFwZ1A4UGE5MlFaV0c5a2NQTjlaM1MxQ3EwVDVQWWRlQV9NWUZPZGZQLVZwaUM5MG5VbDVUYzItS1RlX0RKbG5aeXZUb1hSQWszU3VzVzI1RmhINUQ5WFdEcVdiTEE4MlpwWk5WS0VGbU1hc2JKaUY0OA?oc=5" target="_blank">Clinical and mutational spectrum of paediatric Charcot-Marie-Tooth disease in a large cohort of Chinese patients</a>  <font color="#6f6f6f">Frontiers</font>

Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing
Naturegeneral

Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE16RnBjMEZCR2dhSmtfM0N2V0l4cHFMbkpGa0l2Si1Wa0dySW9sdGdFeW5oSFdjd3NWaWhXWm94WDRfcVcyblBaY2ZDbmhQYUdCX1Rod0JLY3VFb1VTcThR?oc=5" target="_blank">Clinical and genetic spectrum of glycogen storage disease in Iranian population using targeted gene sequencing</a>  <font color="#6f6f6f">Nature</font>

The clinical and genetic spectrum of twenty-six individuals with hearing loss affected by MYO15A variants
Naturegeneral

The clinical and genetic spectrum of twenty-six individuals with hearing loss affected by MYO15A variants

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBaZ2VIR3hnOGJ0Z2dmdVRxdDBia25OeVk0OGhXdjFjZTRLNVVlVVBVNzFoYnB6SHlJSEh0UWdpMm5YZkV5YkhsQXA3OWVqb055ZlRabzdlUGI0VS1IanhJ?oc=5" target="_blank">The clinical and genetic spectrum of twenty-six individuals with hearing loss affected by MYO15A variants</a>  <font color="#6f6f6f">Nature</font>

Expanding the clinical and genetic spectrum of GLUL -related developmental and epileptic encephalopathy
Naturegeneral

Expanding the clinical and genetic spectrum of GLUL -related developmental and epileptic encephalopathy

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1GOEE1aDBRY3VvQ1A1REVTNkJaVUgyX1BXRVprSnYyV3FJREozM19HaHNLVWxNVklxMFozOFplaG5qSWc4eEIwcFZsS3hRUzkxZTlYaVpfekp2MUxSZk53?oc=5" target="_blank">Expanding the clinical and genetic spectrum of GLUL -related developmental and epileptic encephalopathy</a>  <font color="#6f6f6f">Nature</font>

Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease
Naturegeneral

Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBoZEItRVIxMU5XVGlsc0stSGhkT0Z0RGxmdTdWekhMVkdXZlotTTdTRk5hNEpWLXhHdUpxVVVSdXJHbm5ReXR3R3Uzd3I5RUVPNWY4TGFFY3FENnRaN3BF?oc=5" target="_blank">Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease</a>  <font color="#6f6f6f">Nature</font>

Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions | Communications Biology
Naturescience

Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions | Communications Biology

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFA3RFhycWE4b0xMdHA5V2IxVGNyNXdsMWFMRDRwYnlTWXVMck1CU042Qk1PeURxUE5taWJwV3NVZmNHMzdVa3VNdF9JTWpVRTc3NnRTajV6eHRmdnpoNnNn?oc=5" target="_blank">Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions | Communications Biology</a>  <font color="#6f6f6f">Nature</font>

Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran
Natureworld

Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9PWGZSbG1VZkNicDFjdjVRZFNZd0lrNjdjZUwwMEYzdGkyUGRZa3hnSDcyN1hBejBiWklKSGVZZ095MnFqbTdSMjlWclpPRTVIcnlDb3JCdk5sTzJDY1VJ?oc=5" target="_blank">Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran</a>  <font color="#6f6f6f">Nature</font>

Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum
Naturegeneral

Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTE00QXdZaDRGWHBrbklIOWtJUzE1UEc1SjFSM0RNeXJ5M3hIRmtjekxyUjJ0bHp6bkhGWlM2MzNoOU9VVHhCWHZMMWVUaXRGUzNYS2ZN?oc=5" target="_blank">Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum</a>  <font color="#6f6f6f">Nature</font>

Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3 -related anophthalmia and microphthalmia
Naturegeneral

Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3 -related anophthalmia and microphthalmia

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9tc2l6YV83bGNUY3BINU1NelFkUlVtbVFhREprRERZSUhVZjZUcmNaa1JxUm9IYU1sdDA0LTlxdk5RbGxST0RyZVllUzI3dDkwd2FrVTByOTZFUTlfNEZj?oc=5" target="_blank">Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3 -related anophthalmia and microphthalmia</a>  <font color="#6f6f6f">Nature</font>

Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease | European Journal of Human Genetics
Natureworld

Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease | European Journal of Human Genetics

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFA3dWNlUXFNMDJmM3pPblJWMVNjSVdOUDFiT2RUX2FENUZHb2RObnIyaG8xV0Zyay1URTUtLTRLdTFIbTBVb0ZtRE5paVB5N05hYzgwQ3dBMU53eUhZbTlz?oc=5" target="_blank">Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease | European Journal of Human Genetics</a>  <font color="#6f6f6f">Nature</font>

The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children
Frontiersgeneral

The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children

<a href="https://news.google.com/rss/articles/CBMijgFBVV95cUxPWDN4alJuWVlzTEpUWVM0YW1TSE5UNDgtcWpwWHU1Z2JPdUYtUWtUREVxcmlwSzZwZXVjeVA2RDk3V3VWTkZGNjVpQnNwalZnNXpJaVZzZUFIUkdBWUZ2bmhMZ0p3NlhjWk5uTUFJLUpEb0dyaktjTU1Lcms3MU1HSVoydF9LbmZYX0hfZmRn?oc=5" target="_blank">The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children</a>  <font color="#6f6f6f">Frontiers</font>

Unraveling the Overlapping Spectrum of Hereditary Neuropathies: Clinical and Genetic Insights From the UAE
Cureusworld

Unraveling the Overlapping Spectrum of Hereditary Neuropathies: Clinical and Genetic Insights From the UAE

<a href="https://news.google.com/rss/articles/CBMi3AFBVV95cUxNZmpyclJLaC04a1hjR0ZOV1o2dTZIRnFBQm1FYVFIYUIzSnVUM3F2WUkwM1lNWXJqeC1DRkIzcG9pQTZKVEVQcXN6Q1hxdzd3QTFpMklMVGJlVU5EakNoeDUzam1nQ2ZyT1VkQ3laNTE2ZUg4OXdZaV9mRnVFcEc1X0hMMWpQUmJocngwYnc5aE53LWcyVnBYb3BoSVltZm5tX1JWWVJUV0w2MU9xZ0VIWXZzYWVJQnVpS25EUENVYmVCTm9xV1FBYk1OZlFYc3gzUmRzaHhGNDRfZDdt?oc=5" target="_blank">Unraveling the Overlapping Spectrum of Hereditary Neuropathies: Clinical and Genetic Insights From the UAE</a>  <font color="#6f6f6f">Cureus</font>

The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder
Frontiersgeneral

The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder

<a href="https://news.google.com/rss/articles/CBMijwFBVV95cUxQSTR4NWktZG8wYkFFZ1k0NjUyX2JsSzNKMW5ZME4wMVcwQ0pVeXpUZkNQMWhHemx4ZzVMQmpOODJndVo0NWl0bDhmcGtRTFNUSHAtV3V5SU5zU0pmMnZ3amY4U3p6MUhlNko0NXhiYTUzc0U0ZXhnTWRPQzc3Sk1jcGVKSEg0eWYzS292ZVJBQQ?oc=5" target="_blank">The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder</a>  <font color="#6f6f6f">Frontiers</font>

Expanding clinical spectrum of PAICS deficiency: Comprehensive analysis of two sibling cases
Naturetech

Expanding clinical spectrum of PAICS deficiency: Comprehensive analysis of two sibling cases

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9raGotTV96aFhPdUxsR3JyN2VJN3p5Y0NZT05FNjZSaTVyV1o0ekpRX3NkMG1PdXd3X0xscjBUYVQxbG1CQVRJQWxUNnBSLURTSTNJR1BRNDNxRlQzXzhr?oc=5" target="_blank">Expanding clinical spectrum of PAICS deficiency: Comprehensive analysis of two sibling cases</a>  <font color="#6f6f6f">Nature</font>

Autism Spectrum Disorder, 1: Genetic and Environmental Risk Factors
Psychiatrist.comgeneral

Autism Spectrum Disorder, 1: Genetic and Environmental Risk Factors

<a href="https://news.google.com/rss/articles/CBMioAFBVV95cUxPQk5oUm9VeFpldnFSb1pZbzFoNGtyVnF2UmdpY1A1TDMzT2ZvaXVZeXk2aUd6WDJQclZYZjJhTzNVZ05LVEhVcFo2X09VQ1B2ZHJJc1Rpc1FsMDVOMTN4LUgta0ppTWQtRW9HdExBSnhSaFNkU0hOMU0tUEEzQ2xiZUZBaE5DSEtfb1JveTcxOE9jb2l3dy1kQXh5U2tKVzZY?oc=5" target="_blank">Autism Spectrum Disorder, 1: Genetic and Environmental Risk Factors</a>  <font color="#6f6f6f">Psychiatrist.com</font>

Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson’s disease
Naturegeneral

Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson’s disease

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9jZ2NOR1BPSUIyN3dDWjF6VGZyZTl3U09Yb2tHVUNiUXFhVGhVV0Q2bE5IYl84ME5DU2dwOE1NUHpYUFNCblo2WnJNbkFMUXA4X3JTdEMxS0pJdUtEZi1z?oc=5" target="_blank">Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson’s disease</a>  <font color="#6f6f6f">Nature</font>

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations
Naturegeneral

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5sVi1WQko5Q0JfY1lLYS1RZEYwVjBzUHZSWW5LT0d0UlJEeHBHemU1VVl1QUVNd2gxYTBDVWczZTAzQTFiN3EtVFMwM2lBdXQtY0dJMmFYcll5OC11SW13?oc=5" target="_blank">BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations</a>  <font color="#6f6f6f">Nature</font>

New insights into the clinical and molecular spectrum of the MADD -related neurodevelopmental disorder
Naturegeneral

New insights into the clinical and molecular spectrum of the MADD -related neurodevelopmental disorder

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE05X2Uxa3AzYjJ3RWQwYmd5VWtQYnBpaVVsQXBXOG5DdzFnTUx4RTc2UmZWbV9wNUxfeFpPQ0FMR01TTDVZTFQxSV91R2p2bWtkcmZicC1sQ1pUUjNZYnpN?oc=5" target="_blank">New insights into the clinical and molecular spectrum of the MADD -related neurodevelopmental disorder</a>  <font color="#6f6f6f">Nature</font>

Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency
Naturegeneral

Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

<a href="https://news.google.com/rss/articles/CBMiXkFVX3lxTE5saThrREd0dkIxVHp3ekpNLXJSRjBUTlRnQWpneHJwX2pCMU5NLXZ4a29GUG80MGI3NW1wWW1FY3NpbXJ1N2pERTNZZTVhczRDRnVKSWtIdDdOYjc0a1E?oc=5" target="_blank">Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency</a>  <font color="#6f6f6f">Nature</font>

The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome
Naturegeneral

The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9wLVBaQWxZQTdqOUktVnlkSE5NMUZKOUxhSUFEM3QzbjNic0pPd2pYb3ExUHNGZjdzT0NOeEFvWTdXa0VUa2lZSndHaFJnMmVXZlpQaXpCbEtwNVBVR0kw?oc=5" target="_blank">The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome</a>  <font color="#6f6f6f">Nature</font>

"Gene Spectrum and Clinica" — Live Google News Trends & Headlines