PubMed for id: 1633603

Year	Number of Results
1971	1
1973	1
1975	4
1976	2
1977	2
1979	3
1980	5
1981	1
1982	1
1984	2
1985	1
1986	3
1987	3
1988	4
1989	4
1990	3
1991	4
1992	3
1993	10
1994	5
1995	2
1996	12
1997	8
1998	4
1999	7
2000	6
2001	10
2002	13
2003	7
2004	11
2005	13
2006	8
2007	13
2008	11
2009	12
2010	14
2011	14
2012	19
2013	17
2014	14
2015	12
2016	11
2017	14
2018	10
2019	14
2020	17
2021	9
2022	20
2023	16
2024	4

1

Initial clinical and molecular investigation of 20q13.33 microdeletion with 17q25.3/14q32.31q32.33 microduplication in Chinese pediatric patients.

Zhuang J, Zhang N, Wang J, Jiang Y, Zhang H, Chen C. Zhuang J, et al. Mol Genet Genomic Med. 2024 Apr;12(4):e2429. doi: 10.1002/mgg3.2429. Mol Genet Genomic Med. 2024. PMID: 38553934 Free PMC article.

2

A case of mild partial androgen insensitivity syndrome in a juvenile boy.

Wang F, Shao S, He W, Hu S. Wang F, et al. J Int Med Res. 2024 Mar;52(3):3000605241232520. doi: 10.1177/03000605241232520. J Int Med Res. 2024. PMID: 38530023 Free PMC article.

3

Classes and predictors of reversal in male patients with congenital hypogonadotropic hypogonadism: a cross-sectional study of six international referral centres.

Dwyer AA, McDonald IR, Cangiano B, Giovanelli L, Maione L, Silveira LFG, Raivio T, Latronico AC, Young J, Quinton R, Bonomi M, Persani L, Seminara SB, Lee CS. Dwyer AA, et al. Lancet Diabetes Endocrinol. 2024 Apr;12(4):257-266. doi: 10.1016/S2213-8587(24)00028-7. Epub 2024 Mar 1. Lancet Diabetes Endocrinol. 2024. PMID: 38437850

4

Hyperglycemia with hypogonadism and growth hormone deficiency in a 17-year-old male with H syndrome: the first case report from Syria.

Hamsho S, Alaswad M, Sleiay M, Alhusseini A. Hamsho S, et al. BMC Endocr Disord. 2023 Dec 14;23(1):274. doi: 10.1186/s12902-023-01525-w. BMC Endocr Disord. 2023. PMID: 38093297 Free PMC article. Review.

5

Pontocerebellar Hypoplasia 7 with Novel Compound Heterozygous Variants of TOE1 in a Boy with Micropenis, Developmental Delay, and Ataxia: The First Korean Case Report.

Jo YH, Shin KH, Kim H, Lee BL, Chung WY, Lee YJ, Jo HY, Kim YM. Jo YH, et al. Ann Clin Lab Sci. 2023 Sep;53(5):806-810. Ann Clin Lab Sci. 2023. PMID: 37945020

6

Serum steroid metabolite profiling by LC-MS/MS in two phenotypic male patients with HSD17B3 deficiency: Implications for hormonal diagnosis.

Fujisawa Y, Masunaga Y, Tanikawa W, Nakashima S, Ueda D, Sano S, Fukami M, Saitsu H, Yazawa T, Ogata T. Fujisawa Y, et al. J Steroid Biochem Mol Biol. 2023 Nov;234:106403. doi: 10.1016/j.jsbmb.2023.106403. Epub 2023 Sep 22. J Steroid Biochem Mol Biol. 2023. PMID: 37741351

7

A Rare Case of Precocious Puberty in a Child with a Novel GATA-4 Gene Mutation: Implications for Disorders of Sex Development (DSD) and Review of the Literature.

Aversa T, Luppino G, Corica D, Pepe G, Valenzise M, Coco R, Li Pomi A, Wasniewska M. Aversa T, et al. Genes (Basel). 2023 Aug 16;14(8):1631. doi: 10.3390/genes14081631. Genes (Basel). 2023. PMID: 37628683 Free PMC article. Review.

8

[Application of fluorescence in situ hybridization combined with chromosomal karyotyping analysis in children with disorders of sex development due to sex chromosome abnormalities].

Wang G, Wang J, Zhang Z, Li R, Li L, Li D, Zhang W, Zhang Y, Wang M. Wang G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Aug 10;40(8):947-953. doi: 10.3760/cma.j.cn511374-20220810-00535. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37532493 Chinese.

9

Case Report: short stature, kidney anomalies, and cerebral aneurysms in a novel homozygous mutation in the PCNT gene associated with microcephalic osteodysplastic primordial dwarfism type II.

Petraroli M, Percesepe A, Piane M, Ormitti F, Castellone E, Gnocchi M, Messina G, Bernardi L, Patianna VD, Esposito SMR, Street ME. Petraroli M, et al. Front Endocrinol (Lausanne). 2023 May 10;14:1018441. doi: 10.3389/fendo.2023.1018441. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37234811 Free PMC article.

10

Novel LSS variants in alopecia and intellectual disability syndrome: New case report and clinical spectrum of LSS-related rare disease traits.

Elbendary HM, Marafi D, Saad AK, Elhossini R, Duan R, Rafat K, Jhangiani SN, Gibbs RA, Pehlivan D, Calame DG, Posey JE, Lupski JR, Zaki MS. Elbendary HM, et al. Clin Genet. 2023 Sep;104(3):344-349. doi: 10.1111/cge.14348. Epub 2023 May 9. Clin Genet. 2023. PMID: 37157980 Review.

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